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- W2142196472 endingPage "3702" @default.
- W2142196472 startingPage "3699" @default.
- W2142196472 abstract "Abstract C′mon 1,2‐dione : A new diastereo‐ and enantioselective Lewis base catalyzed domino Michael/aldol reaction converts α,β‐unsaturated aldehydes and 1,2‐diones into chiral bicyclo[3.2.1]octane‐6‐carbaldehydes. The products are produced in good to excellent enantioselectivities (90–98 % ee ) and can be transformed into bicyclic diols and triols. Additionally, a retro‐aldol cyclization provides access to valuable tetrahydrochromenones (see scheme). magnified image" @default.
- W2142196472 created "2016-06-24" @default.
- W2142196472 creator A5030473186 @default.
- W2142196472 creator A5039392591 @default.
- W2142196472 creator A5055343267 @default.
- W2142196472 creator A5071153001 @default.
- W2142196472 date "2009-04-28" @default.
- W2142196472 modified "2023-10-18" @default.
- W2142196472 title "Asymmetric Organocatalytic Domino Michael/Aldol Reactions: Enantioselective Synthesis of Chiral Cycloheptanones, Tetrahydrochromenones, and Polyfunctionalized Bicyclo[3.2.1]octanes" @default.
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