Abstract
Continuous-flow aldol-type reactions are the other essential part of the aldol-hydrogenation strategy (Scheme 4.1). In Chap. 2, flow aldol condensation between nitromethane and aldehyde using amine-functionalized SiO2 catalyst was described. To expand the scope of nucleophiles and to access both aldol compounds and dehydrated compounds selectively, I decided to investigate different types of heterogeneous catalysts.
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References
Mukaiyama T (1982) Org. React 28:203; Machajewski TD, Wong C-H (2000) Angew Chem Int Ed 39:1352; Palomo C, Oiarbide M, Garcia JM (2002) Chem Eur J 8:36; Palomo C, Oiarbide M, Garcia JM (2004) Chem Soc Rev 33:65; Schetter B, Mahrwald R (2006) Angew Chem Int Ed 45:7506
Cravotto G, Demetri A, Nano GM, Palmisano G, Penoni A, Tagliapoetra S Eur J (2003) Org Chem 4438; Wang Z, Yin G, Qin J, Gao M, Cao L, Wu A (2008) Synthesis 3675
Tanaka K, Ono N, Kubo A, Kaji A (1979) Synthesis 890
D’Sa BA, Kisanga P, Verkade JG (1998) J Org Chem 63:3961
Yoshikawa N, Yamada YMA, Das J, Sasai H, Shibasaki M (1991) J Am Chem Soc 121:4168
List B, Lerner RA, Barbas CF III (2000) J Am Chem Soc 122:2395
Fuentes A, Marinas JM, Sinisterra JV (1987) Tetrahedron Lett 28:4541
Drexler MT, Amiridis MD (2002) Catal Lett 79:175
Varma RS, Kabalka GW, Evans LT, Pagni RM (1985) Synth Commun 15:279
Climent MJ, Corma A, Iborra S, Primo J (1994) J Catal 151:60
Yamawaki J, Kawate T, Ando T, Hanafusa T (1885) Bull Chem Soc Jpn 1983:56
Shen W, Tompsett GA, Hammond KD, Xing R, Dogan F, Grey CP, Conner WC Jr, Auerbach SM, Huber GW (2011) Appl Catal A 392:57
Tichit D, Lhouty MH, Guida A, Chiche BH, Figueras F, Auroux A, Bartalini D, Garrone E (1995) J Catal 151:50; Guida A, Lhouty MH, Tichit D, Figueras F, Geneste P (1997) Appl Catal A 164:251; Kantam ML, Choudary BM, Reddy ChV, Rao KK, Figueras F (1998) Chem Commun 1033; Rao KK, Gravelle M, Valente JS, Figueras F (1998) J Catal 173:115; Tichit D, Bennani MN, Figueras F, Tessier R, Kervennal J (1998) Appl Clay Sci 13:401; Climent MJ, Corma A, Iborra S, Velty A (2002) Green Chem 4:474; Climent MJ, Corma A, Velty A (2002) Catal Lett 79:157; Climent MJ, Corma A, Iborra S, Velty A (2004) J Catal 221:474; Ebitani K, Motokura K, Mori K, Mizugaki T, Kaneda K (2006) J Org Chem 71:5440
Gelbard G (2005) Ind Eng Chem Res 44:8468
Podrebarac GG, Ng FTT, Rempel GL (1997) Chem Eng Sci 52:2991; Serra-Holm V, Salmi T, Multamaki J, Reinik J, Maki-Arvel P, Sjoholm R, Lindfors LP (2000) Appl Catal A 198:207; Sebti S, Solhy A, Tahir R, Abdelatif S, Boulaajaj S, Mayoral JA, Garcia JI, Fraile JM, Kossir A, Oumimoun H (2003) J Catal 213:1; Shibasaki-Kitagawa N, Honda H, Kuribayashi H, Toda T, Fukumura T, Yonemoto T (2007) Bioresour Technol 98:416; Stevens JG, Bourne RA, Poliakoff M (2009) Green Chem 11:409; Pyo SS, Hedström M, Lundmark S, Rehnberg N, Hatti-Kaul R (2011) Org Process Res Dev 15:631; Bonrath W, Pressel Y, Schutz J, Ferfecki E, Topp KD (2016) ChemCatChem 8:3584
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Saito, Y. (2023). Anion Exchange Resins as Catalysts for Direct Aldol-Type Reactions of Ketones, Esters, and Nitriles Under Continuous-Flow Conditions. In: Multistep Continuous Flow Synthesis of Fine Chemicals with Heterogeneous Catalysts. Springer Theses. Springer, Singapore. https://doi.org/10.1007/978-981-19-7258-4_4
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