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- W2950264952 abstract "An organocatalytic, enantioselective domino Michael-aldol reaction of 2-mercaptobenz-aldehydes with maleimides has been developed. The process, catalyzed by a bifunctional chiral amine thiourea via a hydrogen-bonding mediated activation mechanism using as low as 1 mol % catalyst loading, affords versatile succinimide-containing benzothiopyrans with the generation of 3 stereogenic centers in one single operation." @default.
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- W2950264952 date "2007-12-11" @default.
- W2950264952 modified "2023-09-26" @default.
- W2950264952 title "Chiral Amine Thiourea-Promoted Enantioselective Domino Michael-Aldol Reactions Between 2-Mercaptobenzaldehydes and Maleimides." @default.
- W2950264952 cites W2122816235 @default.
- W2950264952 doi "https://doi.org/10.1002/chin.200750155" @default.
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