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- W2924195181 endingPage "1268" @default.
- W2924195181 startingPage "1253" @default.
- W2924195181 abstract "The development of new strategies for the preparation of chiral amines is an important objective in organic synthesis. In this Synpacts, we summarize our approach for catalytically accessing nucleophilic aminoalkyl metal species from 2-azadienes, and its application in generating a number of important but elusive chiral amine scaffolds. Reductive couplings with ketones and imines afford 1,2-amino tertiary alcohols and 1,2-diamines, respectively, whereas fluoroarylations of gem-difluoro-2-azadienes deliver α-trifluoromethylated benzylic amines. 1 Introduction 2 Background: Umpolung Strategies for Preparing Chiral Amines 3 Background: 2-Azadienes 4 Reductive Couplings of 2-Azadienes 5 Fluoroarylations of gem-Difluoro-2-azadienes 6 Summary and Outlook" @default.
- W2924195181 created "2019-04-01" @default.
- W2924195181 creator A5028206651 @default.
- W2924195181 creator A5042347762 @default.
- W2924195181 creator A5072135340 @default.
- W2924195181 date "2019-03-26" @default.
- W2924195181 modified "2023-09-24" @default.
- W2924195181 title "2-Azadienes as Enamine Umpolung Synthons for the Preparation of Chiral Amines" @default.
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