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Highly Enantioselective Reactions of Cyclohexanone and β,γ-Unsaturated α-Keto Ester: The Tuning of Chemoselectivities by Secondary and Primary Amine Catalysts
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作者 Jianwei Wei Wengang Guo +3 位作者 Xin Zhou Xin Du Yan Liu Can Li 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2014年第10期985-990,共6页
A series of of amphiphilic imidazole based secondary and primary amine catalysts were synthesized and shown to be very effective with an acid cocatalyst for the asymmetric reaction of cyclohexanone to β,γ-unsaturat... A series of of amphiphilic imidazole based secondary and primary amine catalysts were synthesized and shown to be very effective with an acid cocatalyst for the asymmetric reaction of cyclohexanone to β,γ-unsaturated α-keto ester.Interestingly,primary and secondary amine catalysts show different regio-selectivities in this reaction.Under the catalysis of secondary amine 1,excellent enantioselectivities were observed for the products from direct 3+3 reactions of cyclohexanone withβ,γ-unsaturated α-keto esters using water as the solvent.Moreover,the same reactants catalyzed by the primary amines 2 lead to the aldol reactions,affording the corresponding products with high diastereoselectivities and up to 97%ee.Theoretical studies on the transition states by using a model in gas phase revealed that steric effect plays an important role on different chemo-selective induction between the secondary amine 1 and primary amine 2. 展开更多
关键词 emulsion catalysis asymmetric catalysis ORGANOcatalysis
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