Issue 4, 1987

Diastereoselective epoxidation of cis-4-amino allylic alcohol with m-chloroperbenzoic acid. An efficient synthesis of statine

Abstract

Hiroshi Kogen

High diastereoselective epoxidation of cis-4-amino allylic alcohol (3) with m-chloroperbenzoic acid is described and the reaction is applied to teh stereoselective synthesis of the β-hydroxy-γ-amino acid, statine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 311-312

Diastereoselective epoxidation of cis-4-amino allylic alcohol with m-chloroperbenzoic acid. An efficient synthesis of statine

T. Nishi, J. Chem. Soc., Chem. Commun., 1987, 311 DOI: 10.1039/C39870000311

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