Design and synthesis of ludartin derivatives as potential anticancer agents against hepatocellular carcinoma

Abstract

Our previous study demonstrated that guaiane-type sesquiterpenoid ludartin showed potent antihepatoma activity against two human hepatocellular carcinoma cell lines, HepG2 and Huh7, with IC₅₀ values of 32.7 and 34.3 μM, respectively. In this study, 34 ludartin derivatives were designed, synthesized and evaluated for their cytotoxic activities against HepG2 and Huh7 cell lines using an MTT assay in vitro. As a result, 17 compounds increased the activity against HepG2 cells, and 20 compounds enhanced the activity against Huh7 cells; 14 derivatives 2, 4-7, 9, 11, 17, 24, 28-30 and 32-33 were superior to ludartin on both HepG2 and Huh7 cells. In particular, dimeric derivative 33 as the most active compound showed 20-fold and 17-fold enhancement of cytotoxicity against HepG2 and Huh7 cells compared to that of ludartin. These results suggested that compound 33 could serve as a promising lead compound against liver cancer.

Introduction

Hepatocellular carcinoma (HCC) is the second leading cause of cancer-related deaths in the world, with an annual mortality over 4.2 million [1]. HCC can be caused by a variety of factors, including fibrosis and cirrhosis, chronic hepatitis B and C virus infection, aflatoxin infection and alcoholism [2]. The main drugs currently available for the treatment of HCC include the multikinase inhibitors sorafenib, regorafenib, lenvatinib, cabozantinib, and ramucirumab and the immune checkpoint inhibitors nivolumab and pembrolizumab. Recently, combination strategies have become a novel and effective strategy for the treatment of liver cancer (i.e., atezolizumab and bevacizumab) [3]. Icaritin, a prenylated flavonol found in the Epimedium genus, has been approved by the National Medical Products Administration for the treatment of HCC in China [4]. Despite the huge advances have been made in targeted therapy and immunotherapy, the 5-year relative survival rate of patients with HCC for all stages is still lower than 15% [5]. In this context, developing new antihepatoma active molecules with novel structures and different mechanisms of action is highly desirable.

Natural products play a very important role in the discovery of antitumor drugs [6]. Guaianolides, one of the largest subgroups of naturally occurring sesquiterpenoids consisting of a tricyclic 5,7,5-ring system, exhibit significant antitumor activities and have been widely investigated for their potential in the treatment of cancers [7]. Among them, the hydrochloride salt of dimethylamino-arglabin has been developed as an antitumor agent for the treatment of breast, colon, ovarian and lung cancer in Kazakhstan [8]. The fumaric acid salt of dimethylaminomicheliolide [9] and thapsigargin prodrug G-202 [10] are undergoing clinical evaluation for the treatment of malignant tumors.

As one of our ongoing programs to discover antiheptoma sesquiterpenoids from Artemisia species, our previous bioactivity-guided fractionation of A. atrovirens and A. myriantha led to the isolation of 96 antihepatoma sesquiterpenoids, including 67 guaianolides, 15 germacranolides, eight eudesmanolides and two ent-longipinane-type sesquiterpenoids, one xanthanolide and three other sesquiterpenoids [11,12,13,14,15,16,17]. Cytotoxicity studies indicated that guaianolide dimers and mono sesquiterpenoids containing α-methylene-γ-lactones displayed cytotoxicity against HepG2, Huh7, and SMMC-7721 cell lines. Seven compounds exhibited strong cytotoxicity against all three tested cancer cell lines with IC₅₀ values ranging from 3.8 to 9.6 μM being more potent than sorafenib. Especially, lavandiolide H could induce G2/M cell cycle arrest and cause HepG2 cell apoptosis by regulating the expression of Bcl-2 and PARP-1 [11]. Artematrolide A exhibited significant anti-cervical cancer effects via the ROS/ERK/mTOR pathway and a metabolic shift on HeLa S3 and SiHa cells [18]. The synthesis of lavandiolides H, I, and K and artematrolide F via a biomimetic Diels−Alder reaction was accomplished in our laboratory [19]. Ludartin, a 6,12-guaianolide isolated from A. lavandulaefolia [20], exhibited moderate cytotoxicity against HepG2 and Huh7 cell lines with IC₅₀ values of 32.7 and 34.3 μM, respectively. Ludartin was first isolated from A. carruthii [21], which was also found in Stevia yaconensi [22] and other Artemisia species [23,24,25]. The reported investigations have demonstrated that ludartin possesses promising bioactivities, including gastric cytoprotective effects [26], inhibitory action on aromatase [27], activity on TRP ion channels [28], and antiproliferative activity against human tumor cell lines. For instance, ludartin was found to exhibit significant cytotoxicity against T98G, A-549, THP-1, PC-3, HCT-116 and MCF-7 cells in vitro with IC₅₀ values in the range of 0.5–7.5 μM [28, 29]. The anticancer effects of ludartin were associated with the induction of DNA damage and a reduction of mitochondrial membrane potential in MCF-7 cells [30]. Administration of ludartin separately or coadministration with capecitabine effectively inhibited colon tumor growth and angiogenesis in mice [31]. Reported structure–activity relationship (SAR) studies on ludartin involved the synthesis of amino [29] and triazolyl [32,33,34,35,36,] analogs, which indicated that the α, β-unsaturated ketone moiety was a key pharmacophore. Although various pharmacological properties of ludartin have been reported, no investigation of chemically modified ludartin derivatives has been conducted for their antihepatoma effects. In this research, 34 ludartin derivatives were synthesized and evaluated for their cytotoxicity against HepG2 and Huh7 cell lines. The preliminary structure–activity relationships of the synthetic derivatives were also discussed.

Results and discussion

Chemistry

Structurally, ludartin bears a 5,7,5-tricyclic ring system and is characterized by an epoxide on the cyclopentane as well as an exocyclic methylene group conjugated with the carbonyl of the lactone. The synthesis of ludartin derivatives is described in Schemes 1–7. A series of derivatives 1–6 were obtained by epoxide ring opening with different nucleophiles including hydroxide ion, methoxide, formate, fluoride and chloride anions. The hydrolysis of ludartin using a 6% solution of HClO₄ in 1,2-dimethoxyethane delivered diol 1 in 87% yield, and switching the solvent to DMF predominantly formed formylated product 2. Treatment of ludartin with 0.1 M H₂SO₄ in MeOH at room temperature gave methylated compound 3, the addition of methanol selectively took place at the C-4 position. Chlorinated compounds 4-5 were obtained by the reaction of ludartin with TMSCl, while the treatment of ludartin with HF·Py in CH₂Cl₂ gave fluorinated derivative 6. (Scheme 1)

Scheme 1

Reagents and conditions: a 6% HClO₄, DME, r.t., 87%, b HClO₄, DMF, r.t., 76%, c H₂SO₄, MeOH, r.t., 67%, d TMSCl, CH₂Cl₂, r.t., 4 (21%), 5 (42%), e HF·Py, CH₂Cl₂, r.t., 78%

Scheme 2

Reagents and conditions: EDC, DMAP, benzoic acid, appropriate ludartin derivative, CH₂Cl₂, r.t. or reflux, 7 (83%), 8 (76%), 9 (71%), 10 (55%), 11 (83%)

Scheme 3

Reagents and conditions: HCOOH, r.t. 12 (64%); Ac₂O, DMAP, CH₂Cl₂, r.t., 13 (82%); EDC, DMAP, CH₂Cl₂, r.t., 14 (24%), 15 (77%), 16 (87%), 17 (52%), 18 (38%), 19 (42%), 20 (41%), 21 (32%), 22 (90%), 23 (71%), 24 (51%), 25 (95%), 26 (87%), 27 (89%)

Scheme 4

Reagents and conditions: a K₂CO₃, CH₂Cl₂, r.t., S1 (67%), S2 (68%), b compound 1, DCC, DMAP, CH₂Cl₂, r.t., 28 (56%), 29 (88%)

Scheme 5

Reagents and conditions: a compound 1, DCC, DMAP, CH₂Cl₂, r.t., 54%, b CF₃COOH, CH₂Cl₂, r.t., 92% (c) Et₃N, CH₂Cl₂, r.t., 51%

Scheme 6

Reagents and conditions: a EDC, DMAP, CH₂Cl₂, r.t., 77%; b BnBr, K₂CO₃, DMF, 73%

Scheme 7

Reagents and conditions: EDC, DMAP, appropriate carboxylic acid, CH₂Cl₂, r.t., 33 (15%), 34 (48%)

The esterification of sesquiterpenoids with carboxylic acid was proven to be an effective way to enhance their anticancer activity [33]. Thus, compounds 1–3 and 5, 6 were esterified with benzoic acid to obtain derivatives 7–11 (Scheme 2). Since the benzoylation product derived from compound 1 showed the most promising activity against HepG2 cells among compounds 7–11, compound 1 was selected for further 3-O-derivatization studies. The treatment of compound 1 with different carboxylic acids in the presence of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) and 4-dimethylaminopyridine (DMAP) gave compounds 14–27 (Scheme 3). Alkyl-, aryl-, and heterocycle substituted acyl groups were introduced into the C3-position of compound 1, which were evaluated for their cytotoxicity to explore the influence of the ester side chain. It has been demonstrated that the incorporation of an additional Michael receptor into a certain molecule is an effective strategy for enhancing its biological activities [34]. Thus, compounds 28 and 29 containing acrylamide moieties were prepared from compound 1, acryloyl chloride and 4-aminobenzoic acid or 3-aminobenzoic acid in two steps (Scheme 4). To clarify the impact of the substituent at the acrylamide moieties on the activity, compound 30 with β-dimethylaminomethyl substituents was then prepared from 4-(Boc-amino) benzoic acid and (2E)-4-(dimethylamino)but-2-enoyl chloride hydrochloride in three steps (Scheme 5).

Hybridization of natural products with known anticancer agents is an efficient strategy to achieve enhanced activities due to multitargeting features and synergistic effects between the prototype molecules and other anticancer pharmacophores [35, 36]. Thus, a hybrid of ludartin derivative and 5-fluorouracil was synthesized by reaction of compound 1 with 5-fluorouracil-1-yl acetic acid. Alkylation of 31 with benzyl bromide delivered conjugate 32 (Scheme 6). Inspired by the discovery that dimers of sesquiterpenoids such as artemisinin [36] and parthenolide [37] showed elevated anticancer activity, we designed and synthesized two dimers linked by ester bonds. Coupling of 1 with terephthalic acid or succinic acid afforded dimers 33, 34 (Scheme 7).

Biology

The structure and purity of the synthetic compounds (higher than 95%) were demonstrated by ¹H and ¹³C NMR spectroscopic data, and HRESIMS. All the derivatives were assessed for their cytotoxicity against the proliferation of the human hepatocellular carcinoma cell lines HepG2 and Huh7 using the MTT method with sorafenib as a positive control. As shown in Table 1, 17 compounds (2, 4–7, 9, 11–12, 16–17, 22, 24, 28–30, and 32–33) increased the activity against HepG2 cells, and 20 compounds (2, 4–7, 9, 11, 14, 17, 20, 21, 24–30 and 32, 33) enhanced the activity against Huh7 cells; 14 derivatives were superior to ludartin on both HepG2 and Huh7 cells. Fluorine, chlorine, and formate ester substituted derivatives 2, 4–6 displayed higher activity than ludartin with IC₅₀ values ranging from 10.9 to 26.0 μM, and methoxylation product 3 showed similar cytotoxicity with ludartin. Compounds 7 and 9 enhanced the activity after esterification (1 vs 7, 3 vs 9); among them, compound 7 was 5-fold and 2-fold more potent than ludartin against HepG2 and Huh7 cells with IC₅₀ values of 5.9 μM and 16.2 μM, respectively.

Table 1 Cytotoxicity of compounds 1–34 against HepG2 and Huh7 cells

Among aliphatic derivatives, compound 16 with a cyclopentyl moiety exhibited the most potent cytotoxicity against HepG2 cells with an IC₅₀ value of 15.5 μM. For HepG2 cells, the introduction of substituents on the phenyl ring of the ester moiety was detrimental to activity as compared to compound 7. For the trifluoromethyl-substituted compounds, para-substituted derivative 20 was more active than ortho- and meta-substituted derivatives (18 and 19). Pentafluorobenzoyl analog 21 showed a 4-fold increase in cytotoxicity against Huh7 with an IC₅₀ value of 8.1 μM, indicating that a polyfluorinated substituent was favorable. When the benzoyl group (7) was replaced by a cinnamoyl group, the anticancer activity decreased. Further replacing the phenyl moiety of compound 7 with a different heterocyclic ring (24–26) led to a decrease in the antiproliferative efficacy. Compounds 28 and 29 bearing acrylamide structural moieties were 2 to 4 fold more active than ludartin with IC₅₀ values of 7.9 and 9.6 μM (HepG2), 8.5 and 16.6 μM (Huh7), suggesting that the incorporation of an additional unsaturated carbonyl was favorable.

Further modifications based on 28 was performed by introducing an aminomethyl substituent at the β–position of acrylamide afford compound 30. For HepG2 cells, compound 30 exhibited 1.5-fold more potent cytotoxicity than compound 28 with an IC₅₀ value of 5.3 μM, indicating that a β-dimethylaminomethyl (DMAM) substituent on acrylamide was beneficial for promoting cytotoxicity. Compound 27, also containing a dimethylamino group with a fumaric acid linker only showed moderate cytotoxicity. The ludartin-5-fluorouracil hybrids 31 and 32 demonstrated different anticancer activities, and the activity of hybrid 32 (11.6 and 7.9 μM) was more potent than that of 31 (>100 and 78.9 μM). These results suggest that the substituent on the 3-N-5-FU moiety was important for anti-proliferative activity.

For dimeric products, compound 33 with a terephthalic acid linker displayed the most potent activity against both HepG2 and Huh7 cells with IC₅₀ values of 1.6 and 2.0 μM, which was 20-fold and 17-fold more potent than ludartin and was 5-fold and 5-fold higher than the positive control sorafenib. Compound 34 with a succinic acid linker was significantly less potent (30.1 and 35.0 μM), suggesting that the linkers were critical for the cytotoxicity of the dimers.

From the above structure and activity results, preliminary SARs can be drawn: the acyloxys at the C-3 position had a different effect on the activity, and dimeric derivative with a terephthalic acid linker could dramatically increase the activity.

Conclusions

In summary, 34 derivatives of ludartin were synthesized and evaluated for their anti-HCC activity against HepG2 and Huh7 cells. Seventeen derivatives showed higher activities against HepG2 cells with IC₅₀ values superior to ludartin, and 20 compounds increased cytotoxicity against Huh7 cells. The most active compound 33 demonstrated 20-fold and 17-fold improvement compared to ludartin, and was 5-fold and 5-fold more potent than the clinically used anticancer drug sorafenib. These results provide a new insight for the design of ludartin derivatives to enhance the efficacy of candidates.

Experimental

Chemistry

General

All reagents and solvents were obtained from commercial suppliers and used without further purification. All compounds were purified by silica gel (200–300 mesh, Qingdao Makall Group Co., Ltd., Qingdao, China). ¹H NMR and ¹³C NMR spectra were obtained on a 400 or 600 MHz spectrometer (Bruker, Bremerhaven, Germany) with tetramethylsilane as an internal standard. HRMS was measured by a Shimadzu LC/MS-IT-TOF (Shimadzu, Kyoto, Japan). Melting points were obtained on an SGW® X-4B microscopic melting point apparatus (Shanghai Precision & Scientific Instrument Co., Ltd., Shanghai, China). Optical rotations were measured in MeOH, CDCl₃ or acetone with an Autopol VI (Serial #91058) polarimeter (Rudolph Research Analytical, Hackettstown, NJ, USA). The human hepatocellular carcinoma cell lines HepG2 and Huh7 were purchased from Shanghai Jining Biotechnology Co., Ltd. (Shanghai, China) and were cultured in Dulbecco′s Modified Eagle′s Medium (DMEM; Gibco, Thermo Fisher Scientific Co., Ltd., Suzhou, China) supplemented with 10% heat-inactivated fetal bovine serum (FBS; Gibco, Life Technologies, NY, USA).

Synthesis

3α,4β-dihydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (1) To a stirred solution of ludartin (1 g, 4.07 mmol) in 1,2-dimethoxyethane (DME, 50 mL) was added perchloric acid (25 mL, 6% in water) at room temperature. The reaction mixture was stirred for 3 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum. The crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) to yield compound 1 (934 mg, 87% yield) as a white powder. mp 140~142 °C; $[\alpha]^{20}_{D}$ − 0.4 (c 0.093, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.28-2.14 (2H, m, H-2), 3.84 (1H, d, J = 3.8 Hz, H-3), 2.83-2.79 (1H, m, H-5), 3.94 (1H, t, J = 10.2 Hz, H-6), 2.35 (1H, d, J = 17.0 Hz, H-7), 1.87 (1H, br s, H-8), 1.38-1.29 (1H, m, H-8), 2.10-2.15 (2H, m, H-9), 6.16 (1H, d, J = 3.1 Hz, H-13), 5.44 (1H, d, J = 2.8 Hz, H-13), 1.73 (3H, s, H-14), 1.57 (3H, s, H-15); ¹³C NMR (100 MHz, CDCl₃) δ 132.2 (C, C-1), 39.3 (CH₂, C-2), 82.9 (CH, C-3), 83.1 (C, C-4), 54.1 (CH, C-5), 79.0 (CH, C-6), 51.5 (CH, C-7), 25.8 (CH₂, C-8), 34.4 (CH₂, C-9), 134.5 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 118.8 (CH₂, C-13), 24.1 (CH₃, C-14), 23.9 (CH₃, C-15). HRESIMS calcd for C₁₅H₂₁O₄ [M + H]⁺ 265.1434, found 265.1445.

3α-hydroxy-4β-O-formyl-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (2) To a stirred solution of ludartin (25 mg, 0.1 mmol) in DMF (1 mL) two drops of HClO₄ (70%) was added at room temperature. The reaction mixture was stirred for 30 min. Then, it was quenched with saturated NaHCO₃ aqueous solution and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum. The crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) compound 2 (24 mg, 76% yield) as a white powder. mp 199~201 °C; $[\alpha]^{20}_{D}$ + 25.2 (c 0.104, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.97-2.93 (1H, m, H-2), 2.75-2.67 (1H, m, H-2), 4.64 (1H, d, J = 4.4 Hz, H-3), 2.39 (1H, d, J = 17.0 Hz, H-5), 4.04 (1H, t, J = 10.1 Hz, H-6), 2.11-2.06 (1H, m, H-7), 2.34-2.30 (1H, m, H-8), 1.41-1.31 (1H, m, H-8), 2.27-2.20 (2H, m, H-9), 6.17 (1H, d, J = 3.2 Hz, H-13), 5.46 (1H, d, J = 2.9 Hz, H-13), 1.74 (3H, s, H-14), 1.90 (3H, s, H-15), 8.00 (1H, s, H-16); ¹³C NMR (100 MHz, CDCl₃) δ 131.6 (C, C-1), 38.9 (CH₂, C-2), 74.0 (CH, C-3), 93.2 (C, C-4), 55.4 (CH, C-5), 81.7 (CH, C-6), 51.0 (CH, C-7), 25.7 (CH₂, C-8), 34.8 (CH₂, C-9), 132.7 (C, C-10), 139.2 (C, C-11), 170.1 (C, C-12), 118.8 (CH₂, C-13), 24.7 (CH₃, C-14), 19.4 (CH₃, C-15), 160.0 (CH, C-16). HRESIMS calcd for C₁₆H₂₀O₅Na [M + Na]⁺ 315.1203, found 315.1224.

3α-hydroxy-4β-methoxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (3) To a stirred solution of 0.1 M H₂SO₄ in MeOH (2 mL) was added ludartin (100 mg, 0.4 mmol) at room temperature. The reaction mixture was stirred for 10 min. Then, it was quenched with saturated NaHCO₃ aqueous solution and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 15:85) to yield compound 3 (74 mg, 67% yield) as a white powder. mp 162~164 °C; $[\alpha]^{20}_{D}$ − 4.5 (c 0.112, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.84-2.74 (2H, m, H-2), 4.12 (1H, d, J = 4.0 Hz, H-3), 2.30 (1H, d, J = 16.3 Hz, H-5), 4.04 (1H, t, J = 10.1 Hz, H-6), 2.08-2.02 (1H, m, H-7), 2.71-2.64 (1H, m, H-8), 1.41-1.31 (1H, m, H-8), 2.25-2.18 (2H, m, H-9), 6.15 (1H, d, J = 3.2 Hz, H-13), 5.42 (1H, d, J = 2.9 Hz, H-13), 1.73 (3H, s, H-14), 1.58 (3H, s, H-15), 3.26 (3H, s, H-16); ¹³C NMR (100 MHz, CDCl₃) δ 131.6 (C, C-1), 40.0 (CH₂, C-2), 82.3 (CH, C-3), 86.7 (C, C-4), 55.5 (CH, C-5), 73.9 (CH, C-6), 50.9 (CH, C-7), 25.8 (CH₂, C-8), 35.0 (CH₂, C-9), 133.0 (C, C-10), 139.9 (C, C-11), 170.8 (C, C-12), 118.3 (CH₂, C-13), 24.8 (CH₃, C-14), 17.1 (CH₃, C-15), 50.3 (CH₃, C-16). HRESIMS calcd for C₁₆H₂₃O₄ [M + H]⁺ 279.1591, found 279.1596.

3β-chloro-4α-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (4) and 3α-hydroxy-4β-chloro-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (5) To a stirred solution of ludartin (200 mg, 0.8 mmol) in CH₂Cl₂ (5 mL) was added trimethylchlorosilane (TMSCl, 510 µL, 4 mmol) in portions at 0 °C under argon atmosphere. The reaction mixture was allowed to warm to room temperature and stirred overnight before quenching with saturated NaHCO₃ aqueous solution. Then, it was extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum. The crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 5:95) to yield compounds 4 (47 mg, 21% yield) and 5 (95 mg, 42% yield) as a white powder.

Compound 4: mp 147~149 °C; $[\alpha]^{20}_{D}$ + 41.1 (c 0.107, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.92-2.86 (1H, m, H-2), 2.42-2.33 (1H, m, H-2), 4.16 (1H, dd, J = 11.6 Hz, J = 8.2 Hz, H-3), 2.79-2.77 (1H, m, H-5), 3.86 (1H, t, J = 10.2 Hz, H-6), 2.13-2.09 (1H, m, H-7), 2.30-2.26 (2H, m, H-8), 2.70-2.64 (2H, m, H-9), 6.24 (1H, d, J = 3.3 Hz, H-13), 5.53 (1H, d, J = 2.9 Hz, H-13), 1.70 (3H, s, H-14), 1.37 (3H, s, H-15); ¹³C NMR (100 MHz, CDCl₃) δ 133.0 (C, C-1), 39.6 (CH₂, C-2), 63.9 (CH, C-3), 80.7 (C, C-4), 57.0 (CH, C-5), 83.7 (CH, C-6), 49.7 (CH, C-7), 25.6 (CH₂, C-8), 35.0 (CH₂, C-9), 125.8 (C, C-10), 138.3 (C, C-11), 169.4 (C, C-12), 120.0 (CH₂, C-13), 24.1 (CH₃, C-14), 17.5 (CH₃, C-15). HRESIMS calcd for C₁₅H₁₉O₃ClNa [M + Na]⁺ 305.0915, found 305.0923;

Compound 5: mp 189~191 °C; $[\alpha]^{20}_{D}$ + 8.1 (c 0.111, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 3.05-3.02 (2H, m, H-2), 4.16 (1H, d, J = 4.0 Hz, H-3), 2.38 (1H, d, J = 17.8 Hz, H-5), 4.14-4.09 (1H, m, H-6), 2.77-2.71 (1H, m, H-7), 2.30-2.27 (1H, m, H-8), 1.46-1.37 (1H, m, H-8), 2.13-2.07 (2H, m, H-9), 6.20 (1H, d, J = 3.3 Hz, H-13), 5.48 (1H, d, J = 3.0 Hz, H-13), 1.76 (3H, s, H-14), 1.92 (3H, s, H-15); ¹³C NMR (100 MHz, CDCl₃) δ 132.8 (C, C-1), 39.9 (CH₂, C-2), 80.1 (CH, C-3), 80.5 (C, C-4), 50.0 (CH, C-5), 83.6 (CH, C-6), 55.5 (CH, C-7), 25.7 (CH₂, C-8), 35.0 (CH₂, C-9), 131.1 (C, C-10), 139.2 (C, C-11), 170.1 (C, C-12), 119.0 (CH₂, C-13), 25.2 (CH₃, C-14), 25.0 (CH₃, C-15). HRESIMS calcd for C₁₅H₂₀O₃Cl [M + H]⁺ 283.1095, found 283.1113.

3α-hydroxy-4β-fluoro-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (6) To a stirred solution of ludartin (50 mg, 0.2 mmol) in CH₂Cl₂ (2 mL) was added HF·Py (27 μL, 0.3 mmol) at room temperature. The reaction mixture was stirred for 1 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum. The crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 15:85) to yield compound 6 (42 mg, 78% yield) as a white powder. mp 190~192 °C; $[\alpha]^{20}_{D}$ − 14.7 (c 0.109, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.79-2.70 (2H, m, H-2), 4.01-3.98 (1H, m, H-3), 2.39 (1H, d, J = 16.9 Hz, H-5), 3.92 (1H, t, J = 10.2 Hz, H-6), 2.24-2.18 (1H, m, H-7), 2.32-2.25 (1H, m, H-8), 1.40-1.30 (1H, m, H-8), 2.95-2.86 (1H, m, H-9), 2.10-2.05 (1H, m, H-9), 6.15 (1H, d, J = 3.1 Hz, H-13), 5.43 (1H, d, J = 2.8 Hz, H-13), 1.75 (6H, s, H-14, H-15); ¹³C NMR (100 MHz, CDCl₃) δ 132.6 (C, C-1), 39.3 (CH₂, C-2), 81.4 (CH, C-3), 81.5 (C, C-4), 51.7 (CH, C-5), 77.0 (CH, C-6), 53.3 (CH, C-7), 25.7 (CH₂, C-8), 34.8 (CH₂, C-9), 133.1 (C, C-10), 139.5 (C, C-11), 170.2 (C, C-12), 118.6 (CH₂, C-13), 24.6 (CH₃, C-14), 20.2 (CH₃, C-15). HRESIMS calcd for C₁₅H₂₀O₃F [M + H]⁺ 267.1391, found 267.1408.

3α-O-benzoyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (7) To a stirred solution of benzoic acid (73 mg, 0.6 mmol) in CH₂Cl₂ (2 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 105 μL, 0.6 mmol), compound 1 (53 mg, 0.2 mmol) and 4-dimethylaminopyridine (DMAP, 5 mg, 0.04 mmol) at room temperature. Then the reaction mixture was equipped with a reflux condenser, and heated to reflux for 10 h. After cooling to room temperature, the mixture was diluted with water and extracted with ethyl acetate (3 × 5 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum. The crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 10:90) to yield compound 7 (61 mg, 83% yield) as a white powder. mp 88~90 °C; $[\alpha]^{20}_{D}$ + 98.8 (c 0.016, CHCl₃); ¹H NMR (400 MHz, CDCl₃) δ 3.01-2.91 (2H, m, H-2), 5.14 (1H, d, J = 4.6 Hz, H-3), 2.53 (1H, d, J = 17.2 Hz, H-5), 4.06 (1H, t, J = 10.1 Hz, H-6), 2.12-2.06 (1H, m, H-7), 2.34-2.26 (1H, m, H-8), 1.43-1.33 (1H, m, H-8), 2.84-2.77 (1H, m, H-9), 2.24-2.17 (1H, m, H-9), 6.18 (1H, d, J = 3.2 Hz, H-13), 5.47 (1H, d, J = 2.9 Hz, H-13), 1.70 (3H, s, H-14), 1.63 (3H, s, H-15), 8.00-7.97 (2H, m, H-3ʹ, H-7ʹ), 7.45-7.42 (2H, m, H-4ʹ, H-6ʹ), 7.57-7.54 (1H, m, H-5ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 37.4 (CH₂, C-2), 81.6 (CH, C-3), 82.7 (C, C-4), 55.3 (CH, C-5), 82.8 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.2 (C, C-10), 139.3 (C, C-11), 170.1 (C, C-12), 119.1 (CH₂, C-13), 24.4 (CH₃, C-14), 24.3 (CH₃, C-15), 165.8 (C, C-1ʹ), 130.4 (C, C-2ʹ), 129.7 (CH, C-3ʹ, C-7ʹ), 128.6 (CH, C-4ʹ, C-6ʹ), 133.4 (CH, C-5ʹ). HRESIMS calcd for C₂₂H₂₅O₅ [M + H]⁺ 369.1697, found 369.1701.

3α-O-benzoyl-4β-O-formyl-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (8) To a stirred solution of benzoic acid (24 mg, 0.2 mmol) in CH₂Cl₂ (1 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 35 μL, 0.2 mmol), compound 2 (29 mg, 0.1 mmol) and 4-dimethylaminopyridine (DMAP, 2 mg, 0.02 mmol) at room temperature. The reaction mixture was stirred for 4 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 10:90) to yield compound 8 (30 mg, 76% yield) as a white powder. mp 50~52 °C; $[\alpha]^{20}_{D}$ − 50.7 (c 0.108, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.86-2.76 (2H, m, H-2), 5.88 (1H, d, J = 4.7 Hz, H-3), 2.61 (1H, d, J = 18.0 Hz, H-5), 4.13 (1H, t, J = 10.1 Hz, H-6), 3.07-3.04 (1H, m, H-7), 2.17-2.11 (1H, m, H-8), 1.46-1.36 (1H, m, H-8), 2.35-2.24 (2H, m, H-9), 6.21 (1H, d, J = 3.2 Hz, H-13), 5.50 (1H, d, J = 2.9 Hz, H-13), 1.71 (3H, s, H-14), 1.97 (3H, s, H-15), 7.99-7.97 (2H, m, H-3ʹ, H-7ʹ), 7.48-7.43 (2H, m, H-4ʹ, H-6ʹ), 7.59-7.55 (1H, m, H-5ʹ), 8.07 (1H, s, -CHO); ¹³C NMR (100 MHz, CDCl₃) δ 130.6 (C, C-1), 37.2 (CH₂, C-2), 76.8 (CH, C-3), 91.9 (C, C-4), 56.7 (CH, C-5), 81.6 (CH, C-6), 50.7 (CH, C-7), 25.8 (CH₂, C-8), 35.0 (CH₂, C-9), 133.1 (C, C-10), 139.1 (C, C-11), 170.0 (C, C-12), 119.2 (CH₂, C-13), 24.8 (CH₃, C-14), 20.0 (CH₃, C-15), 165.5 (C, C-1ʹ), 130.0 (C, C-2ʹ), 129.7 (CH, C-3ʹ, C-7ʹ), 128.6 (CH, C-4ʹ, C-6ʹ), 133.4 (CH, C-5ʹ), 159.6 (CH, -CHO). HRESIMS calcd for C₂₃H₂₄O₆Na [M + Na]⁺ 419.1465, found 419.1472.

3α-O-benzoyl-4β-methoxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (9) To a stirred solution of benzoic acid (12 mg, 0.1 mmol) in CH₂Cl₂ (2 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 18 μL, 0.1 mmol), compound 3 (15 mg, 0.05 mmol) and 4-dimethylaminopyridine (DMAP, 2 mg, 0.02 mmol) at room temperature. The reaction mixture was stirred for 10 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 10:90) to yield compound 9 (13 mg, 71% yield) as a white powder. mp 138~140 °C; $[\alpha]^{20}_{D}$ − 85.1 (c 0.079, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2,95-2.89 (2H, m, H-2), 5.42 (1H, d, J = 4.9 Hz, H-3), 2.48 (1H, d, J = 17.6 Hz, H-5), 4.13 (1H, t, J = 10.1 Hz, H-6), 2.11-2.05 (1H, m, H-7), 2.76-2.70 (1H, m, H-8), 1.45-1.35 (1H, m, H-8), 2.34-2.22 (2H, m, H-9), 6.19 (1H, d, J = 3.2 Hz, H-13), 5.46(1H, d, J = 2.9 Hz, H-13), 1.70 (3H, s, H-14), 1.59 (3H, s, H-15), 8.01-7.99 (2H, m, H-3ʹ, H-7ʹ), 7.47-7.43 (2H, m, H-4ʹ, H-6ʹ), 7.59-7.56 (1H, m, H-5ʹ), 3.34 (3H, -OMe); ¹³C NMR (100 MHz, CDCl₃) δ 131.7 (C, C-1), 38.0 (CH₂, C-2), 82.1 (CH, C-3), 86.2 (C, C-4), 56.9 (CH, C-5), 76.7 (CH, C-6), 50.5 (CH, C-7), 25.9 (CH₂, C-8), 35.2 (CH₂, C-9), 132.0 (C, C-10), 139.8 (C, C-11), 170.6 (C, C-12), 118.6 (CH₂, C-13), 24.9 (CH₃, C-14), 17.7 (CH₃, C-15), 166.2 (C, C-1ʹ), 130.3 (C, C-2ʹ), 129.7 (CH, C-3ʹ, C-7ʹ), 128.6 (CH, C-4ʹ, C-6ʹ), 133.3 (CH, C-5ʹ), 50.6 (CH₃, -OMe). HRESIMS calcd for C₂₃H₂₆O₅Na [M + Na]⁺ 405.1672, found 405.1679.

3α-O-benzoyl-4β-chloro-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (10) To a stirred solution of benzoic acid (49 mg, 0.4 mmol) in CH₂Cl₂ (5 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 71 μL, 0.4 mmol), compound 5 (42 mg, 0.15 mmol) and 4-dimethylaminopyridine (DMAP, 5 mg, 0.04 mmol) at room temperature. The reaction mixture was stirred for 9 h. The mixture was diluted with water and extracted with ethyl acetate (3 × 5 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) to yield compound 10 (32 mg, 55% yield) as a white powder. mp 72~74 °C; $[\alpha]^{20}_{D}$ − 44.2 (c 0.110, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 3.22-3.11 (2H, m, H-2), 5.44 (1H, d, J = 4.8 Hz, H-3), 2.54 (1H, d, J = 17.7 Hz, H-5), 4.18 (1H, t, J = 9.8 Hz, H-6), 2.83-2.76 (1H, m, H-7), 2.17-2.10 (1H, m, H-8), 1.51-1.40 (1H, m, H-8), 2.38-2.26 (2H, m, H-9), 6.23 (1H, d, J = 3.2 Hz, H-13), 5.51 (1H, d, J = 2.9 Hz, H-13), 1.94 (3H, s, H-14), 1.73 (3H, s, H-15), 8.01-7.98 (2H, m, H-3ʹ, H-7ʹ), 7.48-7.44 (2H, m, H-4ʹ, H-6ʹ), 7.60-7.57 (1H, m, H-5ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 130.2 (C, C-1), 38.1 (CH₂, C-2), 81.9 (CH, C-3), 79.4 (C, C-4), 49.6 (CH, C-5), 83.6 (CH, C-6), 57.2 (CH, C-7), 25.9 (CH₂, C-8), 35.3 (CH₂, C-9), 133.1 (C, C-10), 139.1 (C, C-11), 169.9 (C, C-12), 119.3 (CH₂, C-13), 25.7 (CH₃, C-14), 25.1 (CH₃, C-15), 165.5 (C, C-1ʹ), 130.0 (C, C-2ʹ), 129.8 (CH, C-3ʹ, C-7ʹ), 128.7 (CH, C-4ʹ, C-6ʹ), 133.5 (CH, C-5ʹ). HRESIMS calcd for C₂₂H₂₄O₄Cl [M + H]⁺ 387.1358, found 387.1353.

3α-O-benzoyl-4β-fluoro-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (11) To a stirred solution of benzoic acid (20 mg, 0.16 mmol) in CH₂Cl₂ (1 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 28 μL, 0.16 mmol), compound 6 (21 mg, 0.08 mmol) and 4-dimethylaminopyridine (DMAP, 2 mg, 0.02 mmol) at room temperature. The reaction mixture was stirred for 4 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 15:85) to yield compound 11 (25 mg, 83% yield) as a white powder. mp 53~55 °C; $[\alpha]^{20}_{D}$ − 92.4 (c 0.097, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 3.07-2.93 (2H, m, H-2), 5.29-5.25 (1H, m, H-3), 2.59 (1H, d, J = 17.7 Hz, H-5), 4.01 (1H, t, J = 10.1 Hz, H-6), 2.14-2.09 (1H, m, H-7), 2.82-2.75 (1H, m, H-8), 1.45-1.35 (1H, m, H-8), 2.35-2.22 (2H, m, H-9), 6.20 (1H, d, J = 3.2 Hz, H-13), 5.48 (1H, d, J = 2.9 Hz, H-13), 1.80-1.73 (6H, m, H-14, H-15), 8.00-7.98 (2H, m, H-3ʹ, H-7ʹ), 7.47-7.44 (2H, m, H-4ʹ, H-6ʹ), 7.60-7.57 (1H, m, H-5ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 131.4 (C, C-1), 37.4 (CH₂, C-2), 78.9 (CH, C-3), 81.2 (C, C-4), 51.2 (CH, C-5), 81.3 (CH, C-6), 54.5 (CH, C-7), 25.7 (CH₂, C-8), 34.9 (CH₂, C-9), 133.2 (C, C-10), 139.3 (C, C-11), 169.9 (C, C-12), 118.9 (CH₂, C-13), 24.7 (CH₃, C-14), 20.6 (CH₃, C-15), 165.5 (C, C-1ʹ), 129.9 (C, C-2ʹ), 129.8 (CH, C-3ʹ, C-7ʹ), 128.6 (CH, C-4ʹ, C-6ʹ), 133.5 (CH, C-5ʹ). HRESIMS calcd for C₂₂H₂₄O₄F [M + H]⁺ 371.1653, found 371.1676.

3α-O-formyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (12) Compound 1 (21 mg, 0.08 mmol) was added to formic acid (4 mL) at room temperature. The reaction mixture was stirred for 9 h. Then, it was quenched with saturated NaHCO₃ aqueous solution and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 15:85) to yield compound 12 (15 mg, 64% yield) as a white powder. mp 180~182 °C; $[\alpha]^{20}_{D}$ − 61.4 (c 0.130, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.91-2.87 (1H, m, H-2), 2.23-2.17 (1H, m, H-2), 5.04 (1H, d, J = 4.5 Hz, H-3), 2.43 (1H, d, J = 17.2 Hz, H-5), 3.97 (1H, t, J = 10.2 Hz, H-6), 2.12-2.07 (1H, m, H-7), 2.33-2.25 (1H, m, H-8), 1.40-1.31 (1H, m, H-8), 2.82-2.74 (2H, m, H-9), 6.18 (1H, d, J = 3.2 Hz, H-13), 5.46 (1H, d, J = 3.0 Hz, H-13), 1.72 (3H, s, H-14), 1.54 (3H, s, H-15), 7.99 (1H, s, H-16); ¹³C NMR (100 MHz, CDCl₃) δ 132.4 (C, C-1), 37.1 (CH₂, C-2), 80.6 (CH, C-3), 82.2 (C, C-4), 54.9 (CH, C-5), 82.5 (CH, C-6), 51.2 (CH, C-7), 25.7 (CH₂, C-8), 34.5 (CH₂, C-9), 133.2 (C, C-10), 139.1 (C, C-11), 169.8 (C, C-12), 119.0 (CH₂, C-13), 24.2 (CH₃, C-14), 24.0 (CH₃, C-15), 160.2 (CH, C-16). HRESIMS calcd for C₁₆H₂₁O₅ [M + H]⁺ 293.1384, found 293.1410.

3α-O-acetyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (13) To a stirred solution of compound 1 (21 mg, 0.08 mmol) in CH₂Cl₂ (1 mL) was added acetic anhydride (27 μL, 0.24 mmol) and 4-dimethylaminopyridine (DMAP, 2 mg, 0.02 mmol) at room temperature. The reaction mixture was stirred for 3 h. Then, it was quenched with saturated NaHCO₃ aqueous solution and extracted with ethyl acetate (3×3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 10:90) to yield compound 13 (20 mg, 82% yield) as a white powder. mp 129~131 °C; $[\alpha]^{20}_{D}$ − 62.6 (c 0.109, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.88-2.83 (1H, m, H-2), 2.28-2.25 (1H, m, H-2), 4.92 (1H, d, J = 4.7 Hz, H-3), 2.37 (1H, d, J = 17.2 Hz, H-5), 3.98 (1H, t, J = 10.2 Hz, H-6), 2.22-2.16 (1H, m, H-7), 2.11-2.09 (1H, m, H-8), 1.40-1.30 (1H, m, H-8), 2.79-2.73 (2H, m, H-9), 6.17 (1H, d, J = 3.2 Hz, H-13), 5.46 (1H, d, J = 3.0 Hz, H-13), 1.71 (3H, s, H-14), 1.51 (3H, s, H-15), 2.05 (3H, s, H-2ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.1 (C, C-1), 37.3 (CH₂, C-2), 80.9 (CH, C-3), 82.5 (C, C-4), 55.1 (CH, C-5), 82.8 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.6 (CH₂, C-9), 133.6 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.1 (CH₂, C-13), 24.4 (CH₃, C-14), 24.0 (CH₃, C-15), 170.4 (C, C-1ʹ), 21.4 (CH₃, C-2ʹ). HRESIMS calcd for C₁₇H₂₃O₅ [M + H]⁺ 307.1540, found 307.1555.

General procedure for the synthesis of compounds 14–26

To a stirred solution of acid (0.16 mmol) in CH₂Cl₂ (1 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 28 μL, 0.16 mmol), compound 1 (21 mg, 0.08 mmol) and 4-dimethylaminopyridine (DMAP, 2 mg, 0.02 mmol) at room temperature. The reaction mixture was stirred for 10 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum.

3α-O-acryloyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (14) White powder, 24% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 105~107 °C; $[\alpha]^{20}_{D}$ − 51.2 (c 0.050, acetone); ¹H NMR (400 MHz, CDCl₃) δ 2.92-2.88 (1H, m, H-2), 2.12-2.07 (1H, m, H-2), 5.00 (1H, d, J = 4.7 Hz, H-3), 2.43 (1H, d, J = 17.2 Hz, H-5), 4.00 (1H, t, J = 10.2 Hz, H-6), 2.24-2.22 (1H, m, H-7), 2.33-2.26 (1H, m, H-8), 1.42-1.32 (1H, m, H-8), 2.84-2.75 (2H, m, H-9), 6.19 (1H, d, J = 3.2 Hz, H-13), 5.47 (1H, d, J = 3.0 Hz, H-13), 1.72 (3H, s, H-14), 1.54 (3H, s, H-15), 6.11 (1H, dd, J = 17.3 Hz, J = 10.4 Hz, H-2ʹ), 5.84 (1H, d, J = 10.4 Hz, H-3ʹ), 6.40 (1H, d, J = 17.3 Hz, H-3ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.2 (C, C-1), 37.3 (CH₂, C-2), 81.1 (CH, C-3), 82.6 (C, C-4), 55.2 (CH, C-5), 82.8 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.5 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.1 (CH₂, C-13), 24.4 (CH₃, C-14), 24.1 (CH₃, C-15), 165.5 (C, C-1ʹ), 128.6 (CH, C-2ʹ), 131.2 (CH₂, C-3ʹ). HRESIMS calcd for C₁₈H₂₃O₅ [M + H]⁺ 319.1540, found 319.1556.

3α-O-octanoyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (15) White powder, 77% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 103~105 °C; $[\alpha]^{20}_{D}$ − 50.0 (c 0.130, acetone); ¹H NMR (400 MHz, CDCl₃) δ 2.87-2.83 (1H, m, H-2), 2.22-2.16 (1H, m, H-2), 4.91 (1H, d, J = 4.6 Hz, H-3), 2.36 (1H, d, J = 17.2 Hz, H-5), 3.98 (1H, t, J = 10.2 Hz, H-6), 2.10-2.07 (1H, m, H-7), 1.40-1.32 (2H, m, H-8), 2.79-2.73 (2H, m, H-9), 6.17 (1H, d, J = 3.2 Hz, H-13), 5.45 (1H, d, J = 3.0 Hz, H-13), 1.70 (3H, s, H-14), 1.51 (3H, s, H-15), 6.11 (2H, t, J = 7.4 Hz, H-2ʹ), 1.61-1.57 (2H, m, H-3ʹ), 1.30-1.24 (8H, m, H-4ʹ~7ʹ), 0.86 (3H, t, J = 6.6 Hz); ¹³C NMR (100 MHz, CDCl₃) δ 132.0 (C, C-1), 37.4 (CH₂, C-2), 80.7 (CH, C-3), 82.5 (C, C-4), 55.1 (CH, C-5), 82.8 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.6 (CH₂, C-9), 133.6 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.0 (CH₂, C-13), 24.3 (CH₃, C-14), 24.0 (CH₃, C-15), 173.1 (C, C-1ʹ), 34.7 (CH₂, C-2ʹ), 25.1 (CH₂, C-3ʹ), 29.0 (CH₂, C-4ʹ), 29.1 (CH₂, C-5ʹ), 31.8 (CH₂, C-6ʹ), 22.7 (CH₂, C-7ʹ), 14.2 (CH₃, C-8ʹ). HRESIMS calcd for C₂₃H₃₅O₅ [M + H]⁺ 391.2479, found 391.2495.

3α-O-cyclopentane formyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (16) White powder, 87% yield after chromatography on silica gel (acetone-petroleum ether, 20:80). mp 120~122 °C; $[\alpha]^{20}_{D}$ −72.8 (c 0.081, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.88-2.82 (1H, m, H-2), 2.28-2.25 (1H, m, H-2), 4.90 (1H, d, J = 4.6 Hz, H-3), 2.34 (1H, d, J = 17.3 Hz, H-5), 3.98 (1H, t, J = 10.1 Hz, H-6), 2.22-2.16 (1H, m, H-7), 2.72-2.66 (1H, m, H-8), 1.40-1.30 (1H, m, H-8), 2.80-2.73 (2H, m, H-9), 6.17 (1H, d, J = 3.1 Hz, H-13), 5.45 (1H, d, J = 2.8 Hz, H-13), 1.70 (3H, s, H-14), 1.51 (3H, s, H-15), 2.11-2.06 (1H, m, H-2ʹ), 1.90-1.74 (4H, m, H-3ʹ, H-6ʹ), 1.68-1.54 (4H, m, H-4ʹ, H-5ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 131.9 (C, C-1), 37.4 (CH₂, C-2), 80.5 (CH, C-3), 82.5 (C, C-4), 55.1 (CH, C-5), 82.8 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.6 (CH₂, C-9), 133.6 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.0 (CH₂, C-13), 24.3 (CH₃, C-14), 24.0 (CH₃, C-15), 175.9 (C, C-1ʹ), 44.1 (CH, C-2ʹ), 30.3 (CH₂, C-3ʹ), 25.8 (CH₂, C-4ʹ, C-5ʹ), 29.8 (CH, C-6ʹ). HRESIMS calcd for C₂₁H₂₉O₅ [M + H]⁺ 361.2010, found 361.2013.

3α-O-(4-bromobenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (17) White powder, 52% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 51~53 °C; $[\alpha]^{20}_{D}$ −62.7 (c 0.118, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.99-2.89 (2H, m, H-2), 5.12 (1H, d, J = 4.6 Hz, H-3), 2.51 (1H, d, J = 17.3 Hz, H-5), 4.04 (1H, t, J = 10.1 Hz, H-6), 2.84-2.78 (1H, m, H-7), 2.31-2.29 (1H, m, H-8), 1.42-1.33 (1H, m, H-8), 2.23-2.08 (2H, m, H-9), 6.18 (1H, d, J = 3.2 Hz, H-13), 5.47 (1H, d, J = 2.9 Hz, H-13), 1.70 (3H, s, H-14), 1.60 (3H, s, H-15), 7.83 (2H, d, J = 8.4 Hz, H-3ʹ, H-7ʹ), 7.56 (2H, d, J = 8.4 Hz, H-4ʹ, H-6ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 37.4 (CH₂, C-2), 81.9 (CH, C-3), 82.5 (C, C-4), 55.3 (CH, C-5), 82.7 (CH, C-6), 51.1 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.2 (C, C-10), 139.2 (C, C-11), 170.0 (C, C-12), 119.1 (CH₂, C-13), 24.4 (CH₃, C-14), 24.2 (CH₃, C-15), 165.1 (C, C-1ʹ), 129.2 (C, C-2ʹ), 131.9 (CH, C-3ʹ, C-7ʹ), 131.2 (CH, C-4ʹ, C-6ʹ), 128.3 (C, C-5ʹ). HRESIMS calcd for C₂₂H₂₃O₅BrNa [M + Na]⁺ 469.0621, found 469.0628.

3α-O-(2-trifluoromethylbenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (18) White powder, 38% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 154~156 °C; $[\alpha]^{20}_{D}$ −47.1 (c 0.079, CHCl₃); ¹H NMR (400 MHz, CDCl₃) δ 2.82-2.73 (2H, m, H-2), 5.14 (1H, d, J = 4.5 Hz, H-3), 2.61 (1H, d, J = 17.2 Hz, H-5), 4.00 (1H, t, J = 10.2 Hz, H-6), 2.98-2.92 (1H, m, H-7), 2.31-2.25 (1H, m, H-8), 1.42-1.32 (1H, m, H-8), 2.23-2.10 (2H, m, H-9), 6.18 (1H, d, J = 3.2 Hz, H-13), 5.46 (1H, d, J = 3.0 Hz, H-13), 1.74 (3H, s, H-14), 1.59 (3H, s, H-15), 7.75-7.72 (2H, m, H-3ʹ, H-6ʹ), 7.65-7.58 (2H, m, H-4ʹ, H-5ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 36.9 (CH₂, C-2), 82.7 (CH, C-3), 82.5 (C, C-4), 55.0 (CH, C-5), 83.0 (CH, C-6), 51.5 (CH, C-7), 25.9 (CH₂, C-8), 34.5 (CH₂, C-9), 133.4 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.0 (CH₂, C-13), 24.2 (CH₃, C-14), 24.1 (CH₃, C-15), 166.3 (C, C-1ʹ), 126.9 (C, C-2ʹ), 130.3 (CH, C-3ʹ), 131.3 (C, C-4ʹ), 132.0 (CH, C-5ʹ), 126.8 (CH, C-6ʹ), 131.5 (CH, C-7ʹ), 124.8 (C, CF₃). HRESIMS calcd for C₂₃H₂₃O₅F₃Na [M + Na]⁺ 459.1390, found 459.1396.

3α-O-(3-trifluoromethylbenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (19) White powder, 42% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 65~67 °C; $[\alpha]^{20}_{D}$ −66.8 (c 0.136, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 3.02-2.92 (2H, m, H-2), 5.17 (1H, d, J = 4.6 Hz, H-3), 2.55 (1H, d, J = 17.4 Hz, H-5), 4.05 (1H, t, J = 10.1 Hz, H-6), 2.87-2.81 (1H, m, H-7), 2.36-2.29 (1H, m, H-8), 1.43-1.34 (1H, m, H-8), 2.21-2.09 (2H, m, H-9), 6.20 (1H, d, J = 3.2 Hz, H-13), 5.49 (1H, d, J = 2.9 Hz, H-13), 1.72 (3H, s, H-14), 1.63 (3H, s, H-15), 8.23 (1H, s, H-3ʹ), 8.17 (1H, d, J = 7.8 Hz, H-5ʹ), 7.59 (1H, t, J = 7.8 Hz, H-6ʹ), 7.82 (1H, d, J = 7.7 Hz, H-7ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.5 (C, C-1), 37.4 (CH₂, C-2), 82.3 (CH, C-3), 82.6 (C, C-4), 55.3 (CH, C-5), 82.7 (CH, C-6), 51.1 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.2 (C, C-10), 139.2 (C, C-11), 169.9 (C, C-12), 119.2 (CH₂, C-13), 24.4 (CH₃, C-14), 24.3 (CH₃, C-15), 164.6 (C, C-1ʹ), 131.1 (C, C-2ʹ), 126.6 (CH, C-3ʹ), 131.5 (C, C-4ʹ), 129.7 (CH, C-5ʹ), 129.3 (CH, C-6ʹ), 132.9 (CH, C-7ʹ), 131.1 (C, CF₃) HRESIMS calcd for C₂₃H₂₄O₅F₃ [M + H]⁺ 437.1570, found 437.1585.

3α-O-(4-trifluoromethylbenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (20) White powder, 41% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 82~84 °C; $[\alpha]^{20}_{D}$ −63.8 (c 0.079, CHCl₃); ¹H NMR (400 MHz, CDCl₃) δ 3.03-2.91 (2H, m, H-2), 5.16 (1H, d, J = 4.6 Hz, H-3), 2.54 (1H, d, J = 17.3 Hz, H-5), 4.05 (1H, t, J = 10.1 Hz, H-6), 2.85-2.79 (1H, m, H-7), 2.31-2.27 (1H, m, H-8), 1.44-1.34 (1H, m, H-8), 2.25-2.08 (2H, m, H-9), 6.19 (1H, d, J = 3.2 Hz, H-13), 5.48 (1H, d, J = 2.9 Hz, H-13), 1.71 (3H, s, H-14), 1.62 (3H, s, H-15), 8.09 (2H, d, J = 8.1 Hz, H-3ʹ, H-7ʹ), 7.70 (2H, d, J = 8.1 Hz, H-4ʹ, H-6ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.5 (C, C-1), 37.4 (CH₂, C-2), 82.3 (CH, C-3), 82.5 (C, C-4), 55.3 (CH, C-5), 82.7 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.1 (C, C-10), 139.2 (C, C-11), 170.0 (C, C-12), 119.2 (CH₂, C-13), 24.4 (CH₃, C-14), 24.2 (CH₃, C-15), 164.6 (C, C-1ʹ), 134.5 (C, C-2ʹ), 130.1 (CH, C-3ʹ, C-7ʹ), 125.6 (CH, C-4ʹ, C-6ʹ), 134.9 (C, C-5ʹ), 133.6 (C, CF₃). HRESIMS calcd for C₂₃H₂₄O₅F₃ [M + H]⁺ 437.1570, found 437.1595.

3α-O-(2,3,4,5,6-pentafluorobenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (21) White powder, 32% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 40~42 °C; $[\alpha]^{20}_{D}$ −44.1 (c 0.160, CH₃OH); ¹H NMR (600 MHz, CDCl₃) δ 2.84-2.76 (2H, m, H-2), 5.20 (1H, d, J = 4.6 Hz, H-3), 2.54 (1H, d, J = 17.4 Hz, H-5), 3.99 (1H, t, J = 10.2 Hz, H-6), 2.99-2.95 (1H, m, H-7), 2.30-2.25 (1H, m, H-8), 1.40-1.34 (1H, m, H-8), 2.23-2.19 (1H, m, H-9), 2.12-2.08 (1H, m, H-9), 6.19 (1H, d, J = 3.3 Hz, H-13), 5.47 (1H, d, J = 3.1 Hz, H-13), 1.73 (3H, s, H-14), 1.62 (3H, s, H-15); ¹³C NMR (150 MHz, CDCl₃) δ 132.7 (C, C-1), 37.2 (CH₂, C-2), 82.6 (CH, C-3), 82.3 (C, C-4), 55.0 (CH, C-5), 83.7 (CH, C-6), 51.3 (CH, C-7), 25.8 (CH₂, C-8), 34.6 (CH₂, C-9), 132.9 (C, C-10), 139.1 (C, C-11), 169.9 (C, C-12), 119.2 (CH₂, C-13), 24.3 (CH₃, C-14), 24.1 (CH₃, C-15), 158.3 (C, C-1ʹ). HRESIMS calcd for C₂₂H₂₀O₅F₅ [M + H]⁺ 459.1225, found 459.1235.

3α-O-nicotinoyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (22) White powder, 90% yield after chromatography on silica gel (acetone-petroleum ether, 20:80). mp 167~169 °C; $[\alpha]^{20}_{D}$ −82.1 (c 0.085, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 3.01-2.96 (1H, m, H-2), 2.24-2.18 (1H, m, H-2), 5.17 (1H, d, J = 4.3 Hz, H-3), 2.53 (1H, d, J = 17.2 Hz, H-5), 4.04 (1H, t, J = 10.1 Hz, H-6), 2.14-2.08 (1H, m, H-7), 2.36-2.29 (1H, m, H-8), 1.43-1.33 (1H, m, H-8), 2.94-2.91 (1H, m, H-9), 2.86-2.80 (1H, m, H-9), 6.18 (1H, d, J = 2.9 Hz, H-13), 5.48 (1H, d, J = 2.5 Hz, H-13), 1.71 (3H, s, H-14), 1.61 (3H, s, H-15), 8.31-8.29 (1H, m, H-3ʹ), 7.47-7.43 (1H, m, H-4ʹ), 8.85-8.78 (1H, m, H-5ʹ), 9.24-9.18 (1H, m, H-6ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.6 (C, C-1), 37.3 (CH₂, C-2), 82.3 (CH, C-3), 82.4 (C, C-4), 55.3 (CH, C-5), 82.7 (CH, C-6), 51.1 (CH, C-7), 25.8 (CH₂, C-8), 34.7 (CH₂, C-9), 133.0 (C, C-10), 139.2 (C, C-11), 170.0 (C, C-12), 119.2 (CH₂, C-13), 24.4 (CH₃, C-14), 24.2 (CH₃, C-15), 164.2 (C, C-1ʹ), 123.8 (C, C-2ʹ), 137.8 (CH, C-3ʹ, C-4ʹ), 153.4 (CH, C-5ʹ), 150.8 (CH, C-6ʹ). HRESIMS calcd for C₂₁H₂₄NO₅ [M + H]⁺ 370.1649, found 370.1650.

3α-O-cinnamoyl-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (23) White powder, 71% yield after chromatography on silica gel (acetone-petroleum ether, 20:80). mp 87~89 °C; $[\alpha]^{20}_{D}$ −63.1 (c 0.084, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.96-2.86 (2H, m, H-2), 5.06 (1H, d, J = 4.6 Hz, H-3), 2.47 (1H, d, J = 17.2 Hz, H-5), 4.02 (1H, t, J = 10.1 Hz, H-6), 2.82-2.76 (1H, m, H-7), 2.35-2.27 (1H, m, H-8), 1.42-1.32 (1H, m, H-8), 2.24-2.19 (1H, m, H-9), 2.13-2.08 (1H, m, H-9), 6.19 (1H, d, J = 3.2 Hz, H-13), 5.47 (1H, d, J = 3.0 Hz, H-13), 1.73 (3H, s, H-14), 1.58 (3H, s, H-15), 6.42 (1H, d, J = 16.0 Hz, H-2ʹ), 7.67 (1H, d, J = 16.0 Hz, H-3ʹ), 7.53-7.51 (2H, m, H-5ʹ, H-9ʹ), 7.38-7.36 (3H, m, H-6ʹ, H-7ʹ, H-8ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.1 (C, C-1), 37.5 (CH₂, C-2), 81.0 (CH, C-3), 82.6 (C, C-4), 55.2 (CH, C-5), 82.8 (CH, C-6), 51.2 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.6 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.0 (CH₂, C-13), 24.4 (CH₃, C-14), 24.1 (CH₃, C-15), 166.3 (C, C-1ʹ), 118.2 (CH, C-2ʹ), 145.3 (CH, C-3ʹ), 134.4 (C, C-4ʹ), 128.2 (CH, C-5ʹ, C-9ʹ), 129.0 (CH, C-6ʹ, C-8ʹ), 130.5(CH, C-7ʹ). HRESIMS calcd for C₂₄H₂₇O₅ [M + H]⁺ 395.1853, found 395.1859.

3α-O-(pyridine-4-acryloyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (24) White powder, 51% yield after chromatography on silica gel (methanol- dichloromethane, 2:98). mp 123~125 °C; $[\alpha]^{20}_{D}$ −58.0 (c 0.100, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.98-2.91 (1H, m, H-2), 2.32-2.27 (1H, m, H-2), 5.07 (1H, d, J = 4.6 Hz, H-3), 2.47 (1H, d, J = 17.3 Hz, H-5), 4.02 (1H, t, J = 10.2 Hz, H-6), 2.14-2.08 (1H, m, H-7), 2.25-2.19 (1H, m, H-8), 1.43-1.33 (1H, m, H-8), 2.88-2.76 (2H, m, H-9), 6.19 (1H, d, J = 3.2 Hz, H-13), 5.48 (1H, d, J = 2.9 Hz, H-13), 1.73 (3H, s, H-14), 1.58 (3H, s, H-15), 6.59 (1H, d, J = 16.0 Hz, H-2ʹ), 7.58 (1H, d, J = 16.0 Hz, H-3ʹ), 7.40-7.37 (2H, m, H-5ʹ, H-8ʹ), 8.68-8.65 (2H, m, H-6ʹ, H-7ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.4 (C, C-1), 37.4 (CH₂, C-2), 81.6 (CH, C-3), 82.5 (C, C-4), 55.2 (CH, C-5), 82.7 (CH, C-6), 51.3 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.4 (C, C-10), 139.2 (C, C-11), 170.0 (C, C-12), 119.2 (CH₂, C-13), 24.4 (CH₃, C-14), 24.1 (CH₃, C-15), 165.3 (C, C-1ʹ), 122.1 (CH, C-2ʹ), 142.3 (CH, C-3ʹ), 141.9 (C, C-4ʹ), 123.1 (CH, C-5ʹ, C-8ʹ), 150.6 (CH, C-6ʹ, C-7ʹ). HRESIMS calcd for C₂₃H₂₆NO₅ [M + H]⁺ 396.1805, found 396.1814.

3α-O-(quinoline-7-formyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (25) White powder, 95 % yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 98~100 °C; $[\alpha]^{20}_{D}$ −43.8 (c 0.101, CHCl₃); ¹H NMR (400 MHz, CDCl₃) δ 3.05-2.97 (2H, m, H-2), 5.21 (1H, d, J = 4.5 Hz, H-3), 2.57 (1H, d, J = 17.3 Hz, H-5), 4.10 (1H, t, J = 10.1 Hz, H-6), 2.87-2.83 (1H, m, H-7), 2.35-2.29 (1H, m, H-8), 1.43-1.33 (1H, m, H-8), 2.24-2.18 (1H, m, H-9), 2.12-2.07 (1H, m, H-9), 6.17 (1H, d, J = 3.1 Hz, H-13), 5.46 (1H, d, J = 2.8 Hz, H-13), 1.71 (3H, s, H-14), 1.67 (3H, s, H-15), 8.52 (1H, s, H-3ʹ), 8.28-8.21 (2H, m, H-5ʹ, H-10ʹ), 7.48-7.45 (1H, m, H-6ʹ), 8.99-8.98 (1H, m, H-7ʹ), 8.15-8.13 (1H, m, H-9ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 37.5 (CH₂, C-2), 82.1 (CH, C-3), 82.4 (C, C-4), 55.4 (CH, C-5), 82.7 (CH, C-6), 51.0 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.1 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.0 (CH₂, C-13), 24.4 (CH₃, C-14), 24.1 (CH₃, C-15), 165.3 (C, C-1ʹ), 128.3 (C, C-2ʹ), 131.1 (CH, C-3ʹ), 127.5 (C, C-4ʹ), 137.5 (CH, C-5ʹ), 122.0 (CH, C-6ʹ), 152.6 (CH, C-7ʹ), 150.1 (C, C-8ʹ), 128.9 (CH, C-9ʹ), 129.9 (CH, C-10ʹ). HRESIMS calcd for C₂₅H₂₆NO₅ [M + H]⁺ 420.1805, found 420.1809.

3α-O-(quinoline-2-formyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (26) White powder, 87% yield after chromatography on silica gel (acetone-petroleum ether, 15:85). mp 90~92 °C; $[\alpha]^{20}_{D}$ −57.1 (c 0.165, CHCl₃); ¹H NMR (400 MHz, CDCl₃) δ 3.07-2.99 (2H, m, H-2), 5.26 (1H, d, J = 4.5 Hz, H-3), 2.64 (1H, d, J = 17.4 Hz, H-5), 4.06 (1H, t, J = 10.2 Hz, H-6), 2.84-2.78 (1H, m, H-7), 2.32-2.26 (1H, m, H-8), 1.42-1.32 (1H, m, H-8), 2.22-2.17 (1H, m, H-9), 2.12-2.06 (1H, m, H-9), 6.18 (1H, d, J = 3.2 Hz, H-13), 5.46 (1H, d, J = 2.9 Hz, H-13), 1.70 (6H, s, H-14, H-15), 8.04-8.02 (1H, m, H-4ʹ), 7.79-7.74 (1H, m, H-5ʹ), 7.87-7.85 (1H, m, H-6ʹ), 8.29-8.26 (2H, m, H-7ʹ, H-9ʹ), 7.64-7.61 (1H, m, H-10ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 37.4 (CH₂, C-2), 82.6 (CH, C-3), 82.7 (C, C-4), 55.3 (CH, C-5), 82.7 (CH, C-6), 51.0 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.2 (C, C-10), 139.3 (C, C-11), 170.0 (C, C-12), 119.1 (CH₂, C-13), 24.4 (CH₃, C-14), 24.2 (CH₃, C-15), 164.4 (C, C-1ʹ), 148.0 (C, C-2ʹ), 147.9 (C, C-3ʹ), 130.4 (CH, C-4ʹ), 131.0 (CH, C-5ʹ), 128.7 (CH, C-6ʹ), 127.5 (CH, C-7ʹ), 129.3 (C, C-8ʹ), 137.3 (CH, C-9ʹ), 120.9 (CH, C-10ʹ). HRESIMS calcd for C₂₅H₂₅NO₅Na [M + Na]⁺ 442.1625, found 442.1629.

3α-O-(4-dimethylamino-2-butenoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (27) To a stirred solution of maleic anhydride (49 mg, 0.5 mmol) in CH₂Cl₂ (2 mL), dimethylamine (250 μL, 0.5 mmol, 2.0 M in THF) and 4-dimethylaminopyridine (DMAP, 7 mg, 0.06 mmol) was added at room temperature. The reaction mixture was stirred for 1 h and the solvent was evaporated under vacuum. To a stirred solution of crude residue in CH₂Cl₂ (2 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 86 μL, 0.5 mmol) and compound 1 (26 mg, 0.1 mmol) at room temperature. The reaction mixture was stirred overnight. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 25:75) to yield compound 27 (35 mg, 89 % yield) as a white powder. mp 92~94 °C; [α]_{20 D}−76.0 (c 0.080, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.81-2.74 (2H, m, H-2), 4.98 (1H, d, J = 4.5 Hz, H-3), 2.40 (1H, d, J = 17.2 Hz, H-5), 3.97 (1H, t, J = 10.1 Hz, H-6), 2.92-2.85 (1H, m, H-7), 2.10-2.05 (1H, m, H-8), 1.38-1.29 (1H, m, H-8), 2.27-2.19 (2H, m, H-9), 6.15 (1H, d, J = 3.2 Hz, H-13), 5.45 (1H, d, J = 3.0 Hz, H-13), 1.69 (3H, s, H-14), 1.51 (3H, s, H-15), 6.74 (2H, d, J = 15.3 Hz, H-2ʹ), 7.39 (2H, d, J = 15.3 Hz, H-3ʹ), 3.01 (1H, s, H-5ʹ), 3.11 (1H, s, H-6ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 37.2 (CH₂, C-2), 81.7 (CH, C-3), 82.3 (C, C-4), 55.0 (CH, C-5), 82.7 (CH, C-6), 51.2 (CH, C-7), 25.8 (CH₂, C-8), 34.6 (CH₂, C-9), 133.2 (C, C-10), 139.2 (C, C-11), 170.0 (C, C-12), 119.0 (CH₂, C-13), 24.3 (CH₃, C-14), 24.0 (CH₃, C-15), 165.1 (C, C-1ʹ), 131.1 (CH, C-2ʹ), 134.5 (CH, C-3ʹ), 164.7 (CH, C-4ʹ), 35.9 (CH, C-5ʹ), 37.7 (CH, C-6ʹ). HRESIMS calcd for C₂₁H₂₈NO₆ [M + H]⁺ 390.1911, found 390.1922.

3α-O-(4-acrylamidebenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (28) To a stirred solution of 4-aminobenzoic acid (680 mg, 5 mmol) in CH₂Cl₂ (5 mL) was added K₂CO₃ (1.73 g, 10 mmol) and acryloyl chloride (490 µL, 6 mmol) at 0 °C under an argon atmosphere. The reaction mixture was allowed to warm to room temperature and stirred overnight before it was quenched with water. Then, it was extracted with ethyl acetate (3 × 20 mL). The combined aqueous phases were acidified by 5% HCl aqueous solution and filtered to provide 4-acrylamidobenzoic acid (640 mg, 67% yield) as yellow powder. To a stirred solution of 4-acrylamidobenzoic acid (38 mg, 0.2 mmol) in CH₂Cl₂ (1 mL) was added dicyclohexylcarbodiimide (DCC, 41 mg, 0.2 mmol), compound 1 (26 mg, 0.1 mmol) and 4-dimethylaminopyridine (DMAP, 2 mg, 0.02 mmol) at room temperature. The reaction mixture was stirred overnight. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 10:90) to yield compound 28 (13 mg, 56% yield) as a white powder. mp 120~122 °C; $[\alpha]^{20}_{D}$ −62.4 (c 0.092, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.99-2.92 (2H, m, H-2), 5.11 (1H, d, J = 4.4 Hz, H-3), 2.53 (1H, d, J = 17.2 Hz, H-5), 4.05 (1H, t, J = 10.1 Hz, H-6), 2.86-2.81 (1H, m, H-7), 2.13-2.09 (1H, m, H-8), 1.42-1.37 (1H, m, H-8), 2.31-2.23 (2H, m, H-9), 6.19 (1H, d, J = 3.1 Hz, H-13), 5.49 (1H, d, J = 2.8 Hz, H-13), 1.71 (3H, s, H-14), 1.60 (3H, s, H-15), 7.96-7.94 (2H, m, H-3ʹ, H-7ʹ), 7.71-7.69 (2H, m, H-4ʹ, H-6ʹ), 6.31 (1H, dd, J = 16.8, 10.2 Hz H-9ʹ), 6.47 (1H, d, J = 16.8 Hz, H-10ʹ), 5.80 (1H, d, J = 10.2 Hz, H-10ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.3 (C, C-1), 37.5 (CH₂, C-2), 81.5 (CH, C-3), 82.7 (C, C-4), 55.3 (CH, C-5), 82.9 (CH, C-6), 51.1 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.3 (C, C-10), 139.3 (C, C-11), 170.2 (C, C-12), 119.2 (CH₂, C-13), 24.4 (CH₃, C-14), 24.3 (CH₃, C-15), 163.9 (C, C-1ʹ), 125.9 (C, C-2ʹ), 131.0 (CH, C-3ʹ, C-4ʹ, C-6ʹ, C-7ʹ), 142.5 (C, C-5ʹ), 165.3 (C, C-8ʹ), 119.3 (CH, C-9ʹ), 128.9 (CH₂, C-10ʹ). HRESIMS calcd for C₂₅H₂₈NO₆ [M + H]⁺ 438.1911, found 438.1918.

3α-O-(3-acrylamidebenzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (29) To a stirred solution of 3-aminobenzoic acid (680 mg, 5 mmol) in CH₂Cl₂ (5 mL) was added K₂CO₃ (1.73 g, 10 mmol) and acryloyl chloride (490 µL, 6 mmol) at 0 °C under an argon atmosphere. The reaction mixture was allowed to warm to room temperature and stirred overnight before it was quenched with water. Then, it was extracted with ethyl acetate (3×20 mL). The combined aqueous phases were acidified by 5% HCl aqueous solution and filtered to provide 4-acrylamidobenzoic acid (650 mg, 68% yield) as a yellow powder. In a sealed tube, dicyclohexylcarbodiimide (DCC, 82 mg, 0.4 mmol), compound 1 (53 mg, 0.4 mmol) and 4-dimethylaminopyridine (DMAP, 5 mg, 0.04 mmol) was added to a stirred solution of 3-acrylamidobenzoic acid (76 mg, 0.4 mmol) in CH₂Cl₂ (2 mL) at room temperature. The reaction mixture was heated to 50 °C and stirred for 7 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 25:75) to yield compound 29 (76 mg, 88% yield) as a white powder. mp 111~113 °C; $[\alpha]^{20}_{D}$ −58.6 (c 0.103, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.97-2.86 (2H, m, H-2), 5.06 (1H, d, J = 4.5 Hz, H-3), 2.49 (1H, d, J = 17.2 Hz, H-5), 4.05 (1H, t, J = 10.1 Hz, H-6), 2.74-2.71 (1H, m, H-7), 2.07-2.03 (1H, m, H-8), 1.39-1.29 (1H, m, H-8), 2.29-2.14 (2H, m, H-9), 6.15 (1H, d, J = 2.9 Hz, H-13), 5.45 (1H, d, J = 2.5 Hz, H-13), 1.67 (3H, s, H-14), 1.55 (3H, s, H-15), 8.04 (1H, s, H-3ʹ), 7.68-7.66 (1H, m, H-5ʹ), 7.38-7.34 (1H, m, H-6ʹ), 8.12-8.10 (1H, m, H-7ʹ), 5.73-5.70 (1H, m, H-9ʹ), 6.43-6.30 (1H, m, H-10ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.2 (C, C-1), 37.3 (CH₂, C-2), 81.9 (CH, C-3), 82.2 (C, C-4), 55.1 (CH, C-5), 82.8 (CH, C-6), 50.7 (CH, C-7), 25.7 (CH₂, C-8), 34.6 (CH₂, C-9), 132.7 (C, C-10), 139.2 (C, C-11), 170.5 (C, C-12), 119.1 (CH₂, C-13), 24.4 (CH₃, C-14), 23.8 (CH₃, C-15), 164.2 (C, C-1ʹ), 130.8 (C, C-2ʹ), 120.9 (CH, C-3ʹ), 138.5 (C, C-4ʹ), 125.2 (CH, C-5ʹ), 129.2 (CH, C-6ʹ), 124.8 (CH, C-7ʹ), 165.6 (C, C-8ʹ), 131.1 (CH, C-9ʹ), 128.1 (CH₂, C-10ʹ). HRESIMS calcd for C₂₅H₂₈NO₆ [M + H]⁺ 438.1911, found 438.1917.

3α-O-(4-(1-dimethylamino-2-butenamide)benzoyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (30) To a stirred solution of 4-(tert-butoxycarbonylamino) benzoic acid (355 mg, 1.5 mmol) in CH₂Cl₂ (5 mL) was added dicyclohexylcarbodiimide (DCC, 309 mg, 1.5 mmol), compound 1 (264 mg, 1 mmol) and 4-dimethylaminopyridine (DMAP, 25 mg, 0. 2 mmol) at room temperature. The reaction mixture was stirred overnight. Then, it was quenched with water and extracted with ethyl acetate (3 × 20 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) provided intermediate S3 (263 mg, 54% yield) as a white powder. Trifluoroacetic acid was added to a stirred solution of intermediate S3 (240 mg, 0.7 mmol) in CH₂Cl₂ (3 mL) (1 mL) at room temperature. The reaction mixture was stirred 4 h. Then, it was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate (3 × 20 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) provided intermediate S4 (247 mg, 92% yield) as a white powder. To a stirred solution of acyl chloride in CH₂Cl₂ (3 mL), intermediate S4 (23 mg, 0.06 mmol) and triethylamine (138 µL, 1.0 mmol) were added at room temperature. The reaction mixture was stirred 4 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 20 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) to provide 30 (15 mg, 51% yield) as a white powder. mp 130~132 °C; $[\alpha]^{20}_{D}$ −59.0 (c 0.097, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.98-2.90 (2H, m, H-2), 5.09 (1H, d, J = 4.4 Hz, H-3), 2.50 (1H, d, J = 17.2 Hz, H-5), 4.06 (1H, t, J = 10.1 Hz, H-6), 2.84-2.79 (1H, m, H-7), 1.42-1.33 (2H, m, H-8), 2.19-2.07 (2H, m, H-9), 6.20-6.15 (2H, m, H-13, H-9ʹ), 5.45 (1H, d, J = 2.7 Hz, H-13), 1.70 (3H, s, H-14), 1.58 (3H, s, H-15), 7.92 (2H, d, J = 8.3 Hz, H-3ʹ, H-7ʹ), 7.69 (2H, d, J = 8.4 Hz, H-4ʹ, H-6ʹ), 7.01-6.94 (1H, m, H-10ʹ), 3.09-3.07 (2H, m, H-11ʹ), 2.25 (6H, s, H-12ʹ, H-13ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.2 (C, C-1), 37.5 (CH₂, C-2), 81.6 (CH, C-3), 82.5 (C, C-4), 55.3 (CH, C-5), 82.9 (CH, C-6), 51.1 (CH, C-7), 25.9 (CH₂, C-8), 34.7 (CH₂, C-9), 133.3 (C, C-10), 139.3 (C, C-11), 170.4 (C, C-12), 119.2 (CH₂, C-13), 24.5 (CH₃, C-14), 24.1 (CH₃, C-15), 164.0 (C, C-1ʹ), 125.6 (C, C-2ʹ), 130.9 (CH, C-3ʹ, C-4ʹ, C-6ʹ, C-7ʹ), 142.8 (C, C-5ʹ), 165.5 (C, C-8ʹ), 125.8 (CH, C-9ʹ), 143.2 (CH, C-10ʹ), 60.3 (CH₂, C-11ʹ), 45.6 (CH₃, C-12ʹ, C-13ʹ). HRESIMS calcd for C₂₈H₃₅N₂O₆ [M + H]⁺ 495.2490, found 495.2494.

3α-O-(2,4-dioxo-5-fluoro-3,4-dihydro-1(2H)-pyrimidineacetyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (31) To a stirred solution of 5-fluoro-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidineacetic acid (75 mg, 0.4 mmol) in CH₂Cl₂ (2 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 70 μL, 0.4 mmol), compound 1 (53 mg, 0.2 mmol) and 4-dimethylaminopyridine (DMAP, 5 mg, 0.04 mmol) at room temperature. The reaction mixture was stirred for 22 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 25:75) to provide compound 31 (66 mg, 77% yield) as a white powder. mp 121~123 °C; $[\alpha]^{20}_{D}$ −21.5 (c 0.094, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.29-2.16 (2H, m, H-2), 5.00 (1H, br.s, H-3), 2.36 (1H, d, J = 17.2 Hz, H-5), 3.97 (1H, t, J = 10.1 Hz, H-6), 2.89-2.85 (1H, m, H-7), 2.08-2.05 (1H, m, H-8), 1.37-1.28 (1H, m, H-8), 2.77-2.68 (2H, m, H-9), 6.14 (1H, s, H-13), 5.45 (1H, s, H-13), 1.69 (3H, s, H-14), 1.46 (3H, s, H-15), 4.51-4.39 (2H, m, H-2ʹ), 7.35-7.33 (1H, m, H-6ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.6 (C, C-1), 37.1 (CH₂, C-2), 82.1 (CH, C-3), 82.6 (C, C-4), 54.9 (CH, C-5), 82.9 (CH, C-6), 51.1 (CH, C-7), 25.7 (CH₂, C-8), 34.6 (CH₂, C-9), 132.7 (C, C-10), 139.2 (C, C-11), 170.4 (C, C-12), 119.2 (CH₂, C-13), 24.4 (CH₃, C-14), 23.7 (CH₃, C-15), 166.6 (C, C-1ʹ), 49.3 (CH₂, C-2ʹ), 149.9 (C, C-3ʹ), 157.5 (C, C-4ʹ), 141.7 (C, C-5ʹ), 129.3 (CH, C-6ʹ). HRESIMS calcd for C₂₁H₂₄N₂O₇F [M + H]⁺ 435.1562, found 435.1564.

3α-O-(3-benzyl-2,4-dioxo-5-fluoro-3,4-dihydro-1(2H)-pyrimidineacetyl)-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide (32) To a stirred solution of compound 31 (22 mg, 0.05 mmol) in DMF (1 mL) was added benzyl bromide (12 μL, 0.1 mmol) and K₂CO₃ (28 mg, 0.2 mmol) at room temperature. The reaction mixture was stirred for 10 h. Then, it was quenched with 5% HCl aqueous solution and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 25:75) to yield compound 32 (19 mg, 73% yield) as a white powder. mp 93~95 °C; $[\alpha]^{20}_{D}$ −13.5 (c 0.110, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 2.91-2.85 (1H, m, H-2), 2.62-2.59 (1H, m, H-2), 5.01 (1H, d, J = 4.4 Hz, H-3), 2.38 (1H, d, J = 17.2 Hz, H-5), 3.92 (1H, t, J = 10.1 Hz, H-6), 2.10-2.04 (1H, m, H-7), 2.68-2.63 (1H, m, H-8), 1.38-1.30 (1H, m, H-8), 2.21-2.19 (2H, m, H-9), 6.18 (1H, d, J = 3.2 Hz, H-13), 5.47 (1H, d, J = 3.0 Hz, H-13), 1.72 (3H, s, H-14), 1.46 (3H, s, H-15), 5.16-5.08 (2H, m, H-2ʹ), 7.32-7.26 (3H, m, H-6ʹ, H-9ʹ, H-13ʹ), 4.53 (1H, d, J = 17.4 Hz, H-7ʹ), 4.34 (1H, d, J = 17.4 Hz, H-7ʹ), 7.48-7.46 (2H, m, H-10ʹ, H-12ʹ), 7.20-7.18 (1H, m, H-11ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.8 (C, C-1), 37.1 (CH₂, C-2), 82.4 (CH, C-3), 82.2 (C, C-4), 54.9 (CH, C-5), 82.8 (CH, C-6), 51.3 (CH, C-7), 25.7 (CH₂, C-8), 34.5 (CH₂, C-9), 132.9 (C, C-10), 139.1 (C, C-11), 169.9 (C, C-12), 119.2 (CH₂, C-13), 24.3 (CH₃, C-14), 24.0 (CH₃, C-15), 166.4 (C, C-1ʹ), 50.1 (CH₂, C-2ʹ), 157.1 (C, C-3ʹ), 157.4 (C, C-4ʹ), 150.1 (C, C-5ʹ), 127.0 (CH, C-6ʹ), 45.4 (CH₂, C-7ʹ), 135.9 (C, C-8ʹ), 128.7 (CH, C-9ʹ, C-13ʹ), 129.4 (CH, C-10ʹ, C-12ʹ). HRESIMS calcd for C₂₈H₃₀N₂O₇F [M + H]⁺ 525.2032, found 525.2038.

1,4-bis(3α-hydroxy-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide)phthalate (33) To a stirred solution of terephthalic acid (17 mg, 0.1 mmol) in CH₂Cl₂ (2 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 70 μL, 0.4 mmol), compound 1 (53 mg, 0.2 mmol) and 4-dimethylaminopyridine (DMAP, 5 mg, 0.04 mmol) at room temperature. The reaction mixture was stirred for 10 h. Then, it was quenched with water and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 10:90) to yield compound 33 (10 mg, 15% yield) as a white powder. mp 138~140 °C; $[\alpha]^{20}_{D}$ −89.7 (c 0.117, CH₃OH); ¹H NMR (400 MHz, CDCl₃) δ 3.01-2.97 (2H, m, H-2, H-2ʹ), 2.24-2.20 (2H, m, H-2, H-2ʹ), 5.16 (2H, d, J = 4.5 Hz, H-3, H-3ʹ), 2.55 (2H, d, J = 17.2 Hz, H-5, H-5ʹ), 4.04 (2H, t, J = 10.1 Hz, H-6, H-6ʹ), 2.93-2.90 (2H, m, H-7, H-7ʹ), 2.34-2.27 (2H, m, H-8, H-8ʹ), 1.44-1.34 (2H, m, H-8, H-8ʹ), 2.83-2.78 (2H, m, H-9, H-9ʹ), 2.13-2.11 (2H, m, H-9, H-9ʹ), 6.21 (2H, d, J = 3.2 Hz, H-13, H-13ʹ), 5.49 (2H, d, J = 2.9 Hz, H-13, H-13ʹ), 1.72 (6H, s, H-14, H-14ʹ), 1.62 (6H, s, H-15, H-15ʹ), 8.06 (4H, s, H-18, H-18ʹ, H-19, H-19ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.5 (C, C-1, C-1ʹ), 37.4 (CH₂, C-2, C-2ʹ), 82.1 (CH, C-3, C-3ʹ), 82.6 (C, C-4, C-4ʹ), 55.4 (CH, C-5, C-5ʹ), 82.7 (CH, C-6, C-6ʹ), 51.3 (CH, C-7, C-7ʹ), 25.9 (CH₂, C-8, C-8ʹ), 34.7 (CH₂, C-9, C-9ʹ), 133.2 (C, C-10, C-10ʹ), 139.2 (C, C-11, C-11ʹ), 170.0 (C, C-12, C-12ʹ), 119.3 (CH₂, C-13, C-13ʹ), 24.4 (CH₃, C-14, C-14ʹ), 24.3 (CH₃, C-15, C-15ʹ), 164.9 (C, C-16, C-16ʹ), 134.3 (C, C-17, C-17ʹ), 129.8 (CH, C-18, C-18ʹ, C-19, C-19ʹ). HRESIMS calcd for C₃₈H₄₃O₁₀ [M + H]⁺ 659.2851, found 659.2861.

1,4-bis(3α-hydroxy-4β-hydroxy-5,7α,6β(H)-guaia-1(10),11(13)-dien-12,6-olide)succinate (34) To a stirred solution of succinic acid (73 mg, 0.6 mmol) in CH₂Cl₂ (1 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 21 μL, 0.12 mmol), compound 1 (32 mg, 0.12 mmol) and 4-dimethylaminopyridine (DMAP, 3 mg, 0.025 mmol) at room temperature. Then the reaction mixture was equipped with a reflux condenser, and heated to 50 °C for 24 h. After cooling to room temperature, the mixture was diluted with saturated NaHCO₃ aqueous solution and extracted with ethyl acetate (3 × 3 mL). The combined organic phases were washed with brine, dried over anhydrous Na₂SO₄, filtered and evaporated under vacuum, the crude residue was purified by silica gel column chromatography (acetone-petroleum ether, 20:80) to yield compound 34 (15 mg, 48% yield) as a white powder. mp 97~99 °C; $[\alpha]^{20}_{D}$ + 48.3 (c 0.012, CHCl₃); ¹H NMR (400 MHz, CDCl₃) δ 2.88-2.84 (2H, m, H-2, H-2ʹ), 2.22-2.17 (2H, m, H-2, H-2ʹ), 4.94 (2H, d, J = 4.6 Hz, H-3, H-3ʹ), 2.37 (2H, d, J = 17.2 Hz, H-5, H-5ʹ), 3.97 (2H, t, J = 10.1 Hz, H-6, H-6ʹ), 2.11-2.09 (2H, m, H-7, H-7ʹ), 2.53-2.26 (2H, m, H-8, H-8ʹ), 1.40-1.31 (2H, m, H-8, H-8ʹ), 2.80-2.74 (4H, m, H-9, H-9ʹ), 6.18 (2H, d, J = 3.2 Hz, H-13, H-13ʹ), 5.47 (2H, d, J = 2.9 Hz, H-13, H-13ʹ), 1.71 (6H, s, H-14, H-14ʹ), 1.51 (6H, s, H-15, H-15ʹ), 2.61 (4H, s, H-17, H-17ʹ); ¹³C NMR (100 MHz, CDCl₃) δ 132.2 (C, C-1, C-1ʹ), 37.3 (CH₂, C-2, C-2ʹ), 81.2 (CH, C-3, C-3ʹ), 82.5 (C, C-4, C-4ʹ), 55.1 (CH, C-5, C-5ʹ), 82.7 (CH, C-6, C-6ʹ), 51.2 (CH, C-7, C-7ʹ), 25.9 (CH₂, C-8, C-8ʹ), 34.7 (CH₂, C-9, C-9ʹ), 133.4 (C, C-10, C-10ʹ), 139.2 (C, C-11, C-11ʹ), 170.0 (C, C-12, C-12ʹ), 119.2 (CH₂, C-13, C-13ʹ), 24.4 (CH₃, C-14, C-14ʹ), 24.1 (CH₃, C-15, C-15ʹ), 171.5 (C, C-16, C-16ʹ), 29.5 (C, C-17, C-17ʹ). HRESIMS calcd for C₃₄H₄₂O₁₀Na [M + Na]⁺ 633.2670, found 633.2678.

Cytotoxicity assay

The cytotoxicity of the compounds was tested by the MTT assay. Briefly, cells at a density of 3 × 104 cells/well were seeded into 96-well plates and incubated at 37 °C with 5% CO₂ for 24 h. The culture medium was replaced with fresh medium containing different concentrations of compound, and the cells were incubated for an additional 48 h. After removal of the medium, 100 μL of MTT reagent (1 mg/mL) was added to each well, and the plates were kept in an incubator for 4 h. After that, 100 μL of dimethyl sulfoxide (DMSO) was added to each well, and the plates were measured at 490 nm using a microplate reader (BIO-RAD, USA). The inhibitory ratio was calculated as [(A_{490 control} − A_{490 treated})/A_{490 control}] × 100%. The cytotoxicity of compounds was expressed as IC₅₀ values calculated by GraphPad Prism 5 (GraphPad Software, California, USA).