Erythropel HC, Zimmerman JB, de Winter TM, Petitjean L, Melnikov F, Lam CH, Lounsbury AW, Mellor KE, Janković NZ, Tu Q, Pincus LN, Falinski MM, Shi W, Coish P, Plata DL, Anastas PT (2018) The green ChemisTREE: 20 years after taking root with the 12 principles. Green Chem 20:1929–1961. https://doi.org/10.1039/C8GC00482J
CAS
Article
Google Scholar
Singh MS, Chowdhury S (2012) Recent developments in solvent-free multicomponent reactions: a perfect synergy for eco-compatible organic synthesis. RSC Adv 2:4547–4592. https://doi.org/10.1039/C2RA01056A
CAS
Article
Google Scholar
Martins MAP, Frizzo CP, Moreira DN, Buriol L, Machado P (2009) Solvent-free heterocyclic synthesis. Chem Rev 109:4140–4182. https://doi.org/10.1021/cr9001098
CAS
Article
PubMed
Google Scholar
Graaff C, Ruijter E, Orru R (2012) Recent developments in asymmetric multicomponent reactions. Chem Soc Rev 41:3969–4009. https://doi.org/10.1039/C2CS15361K
Article
PubMed
Google Scholar
Manley B, Anastas PT, Cue BW (2008) Frontiers in green chemistry: meeting the grand challenges for sustainability in R&D and manufacturing. J Clean Prod 16:743–750. https://doi.org/10.1016/j.jclepro.2007.02.025
Article
Google Scholar
Brauch S, Berkel SSV, Westermann B (2013) Higher-order multicomponent reactions: beyond four reactants. Chem Soc Rev 42:4948–4962. https://doi.org/10.1039/C3CS35505E
CAS
Article
PubMed
Google Scholar
Ramon DJ, Yus M (2005) Asymmetric multicomponent reactions (AMCRs): the new frontier. Angew Chem Int Ed 44:1602–1634. https://doi.org/10.1002/anie.200460548
CAS
Article
Google Scholar
Tietze LF, Brasche G, Gericke KM (2006) Domino reactions in organic synthesis. Wiley, Weinheim. ISBN 978-3-527-29060-4
Book
Google Scholar
Tietze LF, Brazel CC, Holsken S, Magull J, Ringe A (2008) Total synthesis of polyoxygenated cembrenes. Angew Chem Int Ed 47:5246–5249. https://doi.org/10.1002/anie.200800626
CAS
Article
Google Scholar
Nicolaou KC, Edmonds DJ, Bulger PG (2006) Cascade reactions in total synthesis. Angew Chem Int 45:7134–7186. https://doi.org/10.1002/anie.200601872
CAS
Article
Google Scholar
Parikh PK, Marvaniya HM, Sen DJ (2011) Chemistry of bioactive tricyclic fused heterocyclic ring having one heteroatom. Int J Drug Dev Res 3:44–50
CAS
Google Scholar
Khan MF, Alam MM, Verma G, Akhtar W, Akhter M, Shaquiquzzaman M (2016) The therapeutic voyage of pyrazole and its analogs: a review. Eur J Med Chem 120:170–201. https://doi.org/10.1016/j.ejmech.2016.04.077
CAS
Article
PubMed
Google Scholar
Karrouchi K, Radi S, Ramli Y, Taoufik J, Mabkhot YN, Al-aizari FA, Ansar M (2018) Synthesis and pharmacological activities of pyrazole derivatives: a review. Molecules 23:134–219. https://doi.org/10.3390/molecules23010134
CAS
Article
PubMed Central
Google Scholar
Faria JV, Vegi PF, Carvalho Miguita AG, dos Santos MS, Rolim Bernardino AM (2017) Recently reported biological activities of pyrazole compounds. Bioorg Med Chem 25:5891–5903. https://doi.org/10.1016/j.bmc.2017.09.035
CAS
Article
PubMed
Google Scholar
Kumar V, Kaur K, Gupta GK, Sharma AK (2013) Pyrazole containing natural products: synthetic preview and biological significance. Eur J Med Chem 69:735–753. https://doi.org/10.1016/j.ejmech.2013.08.053
CAS
Article
PubMed
Google Scholar
Kumar S, Bawa S, Drabu S, Kumar R, Gupta H (2009) Biological activities of pyrazoline derivatives a recent development. Recent Pat Antiinfect Drug Discov 4:154–163. https://doi.org/10.2174/157489109789318569
CAS
Article
PubMed
Google Scholar
Küçükgüzel SG, Şenkardeş S (2015) Recent advances in bioactive pyrazoles. Eur J Med Chem 97:786–815. https://doi.org/10.1016/j.ejmech.2014.11.059
CAS
Article
PubMed
Google Scholar
DeRosa TF (2006) Pyrazoles. In: Derosa TF (ed) Advances in synthetic organic chemistry and methods reported in US patents. Elsevier Science, Amsterdam. ISBN: 9780080444741
Wiley RH, Behr LC, Fusco R, Jarboe CH (1967) The chemistry of heterocyclic compounds: pyrazoles, pyrazolines, pyrazolidines, indazoles and condensed rings. Wiley, New York
Book
Google Scholar
Aggarwal R, Kumar V, Kumar R, Singh SP (2011) Approaches towards the synthesis of 5-aminopyrazoles. Beilstein J Org Chem 7:179–197. https://doi.org/10.3762/bjoc.7.25
CAS
Article
PubMed
PubMed Central
Google Scholar
Shaabani A, Nazeri MT, Afshari R (2018) 5-Amino-pyrazoles: potent reagents in organic and medicinal synthesis. Mol Divers. https://doi.org/10.1007/s11030-018-9902-8
Article
PubMed
Google Scholar
Breytenbach JC, Van Dyk S, Vanden Heever I, Allin SM, Hodkinson CC, Northfield CJ, Page MI (2000) Synthesis and antimicrobial activity of some isoindolin-1-ones derivatives. Bioorg Med Chem Lett 10:1629–1631. https://doi.org/10.1016/S0960-894X(00)00306-1
CAS
Article
PubMed
Google Scholar
Sun C, Xu B (2008) A tandem elimination-cyclization-suzuki approach: efficient one-pot synthesis of functionalized (z)-3-(arylmethylene) isoindolin-1-ones. J Org Chem 18:7361–7364. https://doi.org/10.1021/jo801219j
CAS
Article
Google Scholar
Maugeri C, Alisi MA, Apicella C, Cellai L, Dragone P, Fioravanzo E, Florio S, Furlotti G, Mangano G, Ombrato R, Luisi R, Pompei R, Rincicotti V, Russo V, Vitiello M, Cazzolla N (2008) New anti-viral drugs for the treatment of the common cold. Bioorg Med Chem 16:3091–3107. https://doi.org/10.1016/j.bmc.2007.12.030
CAS
Article
PubMed
Google Scholar
Anzini M, Cappelli A, Vomero S, Giorgi G, Langer T, Bruni G, Romeo MK, Basile AS (1996) Molecular basis of peripheral vs central benzodiazepine receptor selectivity in a new class of peripheral benzodiazepine receptor ligands related to alpidem. J Med Chem 39:4275–4284. https://doi.org/10.1021/jm960325j
CAS
Article
PubMed
Google Scholar
Lu N, Wang L, Li Z, Zhang W (2012) A concise synthesis of 3-(1-alkenyl)isoindolin-1-ones and 5-(1-alkenyl)pyrrol-2-ones by the intermolecular coupling reactions of N-acyliminium ions with unactivated olefins. Beilstein J Org Chem 8:192–200. https://doi.org/10.3762/bjoc.8.21
CAS
Article
PubMed
PubMed Central
Google Scholar
Tian Y, Sun J, Zhang K, Li G, Xu F (2018) Catalyst-free synthesis of 3-(2-quinolinemethylene)-substituted isoindolinones in water. Synthesis 50:2255–2265. https://doi.org/10.1055/s-0037-1609491
CAS
Article
Google Scholar
Chien TC, Chen CS, Yu FH, Chern JW (2004) Nucleosides XI. Synthesis and antiviral evaluation of 5′-alkylthio-5′-deoxy quinazolinone nucleoside derivatives as s-adenosyl-l-homocysteine analogs. Chem Pharm Bull 52:1422–1426. https://doi.org/10.1248/cpb.52.1422
CAS
Article
Google Scholar
Henderson EA, Bavetsias V, Theti DS, Wilson SC, Clauss R, Jackman AL (2006) Targeting the α-folate receptor with cyclopenta[g]quinazoline-based inhibitors of thymidylate synthase. Bioorg Med Chem 14:5020–5042. https://doi.org/10.1016/j.bmc.2006.03.001
CAS
Article
PubMed
Google Scholar
Leamon CP, Low PS (1994) Selective targeting of malignant cells with cytotoxin-folate conjugates. J Drug Target 2:101–112. https://doi.org/10.3109/10611869409015898
CAS
Article
PubMed
Google Scholar
Rohini R, Shanker K, Reddy PM, Ravinder V (2009) Mono and bis-6-arylbenzimidazo[1,2-c]quinazolines: a new class of antimicrobial agents. Eur J Med Chem 44:3330–3339. https://doi.org/10.1016/j.ejmech.2009.03.022
CAS
Article
PubMed
Google Scholar
Kumar A, Rajput CS (2009) Synthesis and anti-inflammatory activity of newer quinazolin-4-one derivatives. Eur J Med Chem 44:83–90. https://doi.org/10.1016/j.ejmech.2008.03.018
CAS
Article
PubMed
Google Scholar
Bekhit AA, Khalil MA (1998) Non-steroidal anti-inflammatory agents: synthesis of novel benzopyrazolyl, benzoxazolyl and quinazolinyl derivatives of 4(3H)-quinazolinones. Pharmazie 53:539–543
CAS
PubMed
Google Scholar
Deetz MJ, Malerich JP, Beatty AM, Smith BD (2001) One-step synthesis of 4(3H)-quinazolinones. Tetrahedron Lett 42:1851–1854. https://doi.org/10.1016/S0040-4039(01)00096-X
CAS
Article
Google Scholar
Khosropour AR, Mohammadpoor-Baltork I, Ghorbankhani H (2006) Bi(TFA)3–[nbp]FeCl4: a new, efficient and reusable promoter system for the synthesis of 4(3H)-quinazolinone derivatives. Tetrahedron Lett 47:3561–3564. https://doi.org/10.1016/j.tetlet.2006.03.079
CAS
Article
Google Scholar
Limbach PA, Crain PF, Mc Closkey JA (1994) Summary: the modified nucleosides of RNA. Nucleic Acids Res 22:2183–2196. https://doi.org/10.1093/nar/22.12.2183
CAS
Article
PubMed
PubMed Central
Google Scholar
Joffe AM, Farley JD, Linden D, Goldsand G (1989) Trimethoprim-sulfamethoxazole-associated aseptic meningitis: case reports and review of the literature. Am J Med 87:332–338. https://doi.org/10.1016/S0002-9343(89)80160-3
CAS
Article
PubMed
Google Scholar
Rosemeyer H (2004) The chemodiversity of purine as a constituent of natural products. Chem Biodivers 1:361–401. https://doi.org/10.1002/cbdv.200490033
CAS
Article
PubMed
Google Scholar
Liu V, Mackool BT (2009) Mycophenolate in dermatology. J Dermatol Treat 141:203–211. https://doi.org/10.1080/09546630310016826
CAS
Article
Google Scholar
Dzierzbicka K, Trzonkowski P, Sewerynek P, Myśliwski A (2003) Synthesis and cytotoxic activity of conjugates of muramyl and normuramyl dipeptides with batracylin derivatives. J Med Chem 46:978–986. https://doi.org/10.1021/jm021067v
CAS
Article
PubMed
Google Scholar
Abdel-Latif FF, El-Shaieb KM, El-Deen AG (2011) An efficient and simple route to prospective biologically active isoindoloquinazoline, pyrimidine and thiazine derivatives using 2-amino-N-arylbenzamidine and related compounds as starting materials. Z Naturforsch B 66:965–971. https://doi.org/10.1515/znb-2011-0916
CAS
Article
Google Scholar
El-Tamany EH, Sowellim SZ, Hamed AA, Radwan AS (2015) Synthesis and antimicrobial activity of some isoindole derivatives. Res Chem Intermed 41:2675–2685. https://doi.org/10.1007/s11164-013-1378-7
CAS
Article
Google Scholar
Gao L, Song Y, Zhang X, Guo S, Fan X (2014) Copper-catalyzed tandem reactions of 2-bromobenzaldehydes/ketones with aminopyrazoles toward the synthesis of pyrazolo[1,5-a]quinazolines. Tetrahedron Lett 55:4997–5002. https://doi.org/10.1016/j.tetlet.2014.07.028
CAS
Article
Google Scholar
Verma AK, Jha RR, Sankar V, Singh RP (2013) Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet-Spengler reaction. Tetrahedron Lett 54:5984–5990. https://doi.org/10.1016/j.tetlet.2013.08.052
CAS
Article
Google Scholar
Shekarrao K, Kaishap PP, Saddanapu V, Addlagatta A, Gogoi S, Boruah R (2014) Microwave-assisted palladium mediated efficient synthesis of pyrazolo[3,4-b]pyridines, pyrazolo[3,4-b]quinolines, pyrazolo[1,5-a]pyrimidines and pyrazolo[1,5-a]quinazolines. RSC Adv 4:24001–24006. https://doi.org/10.1039/C4RA02865A
CAS
Article
Google Scholar
Rahmati A, Alizadeh-Kouzehrash M (2011) Synthesis of N-Alkyl-2-aryl-5H-imidazo[1,2-b]pyrazol-3-amines by a three-component condensation reaction. Synthesis 18:2913–2920. https://doi.org/10.1055/s-0030-1260154
CAS
Article
Google Scholar
Rahmati A, Eskandari M, Alizadeh-Kouzehrash M (2013) Synthesis of 3-(benzylideneamino)-2-phenyl-5H-imidazo[1,2-b]pyrazole-7-carbonitriles via a four- component condensation reaction. Tetrahedron 69:4199–4204. https://doi.org/10.1016/j.tet.2013.03.103
CAS
Article
Google Scholar
Rahmati A, Alizadeh-Kouzehrash M (2019) A four-component reaction: regio- and chemoselective formation of 7-amino-2-(tert-butyl)-5-aryl-4,5-dihydropyrazolo[1,5-a]pyrimidine-6-carbonitrile. Mol Divers. https://doi.org/10.1007/s11030-019-09976-x
Article
PubMed
Google Scholar
Wade LG (2013) Organic chemistry, 8th edn. M A Pearson, Boston. ISBN-13: 978-0321768414