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- W2333426455 endingPage "17893" @default.
- W2333426455 startingPage "17886" @default.
- W2333426455 abstract "The first enantioselective methodology for the synthesis of electron-poor 2-hydroxyalkyl- and 2-aminoalkyl furanes is demonstrated in this study. It utilizes a highly stereoselective organocatalytic one-pot reaction cascade: epoxidation or aziridination of α,β-unsaturated aldehydes followed by Feist−Bénary reaction of various 1,3-dicarbonyl compounds to give the target furanes. This efficient multibond forming reaction cascade benefits from low catalyst loadings and readily available starting materials. Furthermore, the possibility to interrupt the reaction sequence at the stage of the corresponding optically active 2-hydroxyalkyl- and 2-aminoalkyl 2,3-dihydrofuranes with three stereogenic centers is also presented. Finally, models which account for the formation of the optically active 2,3-dihydrofuranes are proposed." @default.
- W2333426455 created "2016-06-24" @default.
- W2333426455 creator A5030044825 @default.
- W2333426455 creator A5045998207 @default.
- W2333426455 creator A5049324354 @default.
- W2333426455 creator A5068263941 @default.
- W2333426455 date "2010-11-30" @default.
- W2333426455 modified "2023-10-18" @default.
- W2333426455 title "An Organocatalytic Approach to 2-Hydroxyalkyl- and 2-Aminoalkyl Furanes" @default.
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