Issue 5, 2000

Some recent applications of α-amino nitrile chemistry

Abstract

Bifunctional α-amino nitriles are not only versatile intermediates in organic synthesis but also exhibit a valuable dual reactivity, which has been utilized in a broad range of synthetic applications. This review highlights recent developments in the chemistry of α-amino nitriles, including asymmetric synthesis of α-amino acids via Strecker reactions using chiral auxiliaries and catalysts, α-amino nitriles as masked iminium ion equivalents in cationic reactions and the synthesis of natural products and heterocycles, and α-metallation to provide nucleophilic acyl anion equivalents and applications to asymmetric Umpolung reactions.

Article information

Article type
Review Article
Submitted
24 May 2000
First published
07 Aug 2000

Chem. Soc. Rev., 2000,29, 359-373

Some recent applications of α-amino nitrile chemistry

D. Enders and J. P. Shilvock, Chem. Soc. Rev., 2000, 29, 359 DOI: 10.1039/A908290E

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