Issue 15, 1993

Oxidation of α-diazoketones derived from L-amino acids and dipeptides using dimethyldioxirane. Synthesis and reactions of homochiral N-protected α-amino glyoxals

Abstract

Homochiral N-protected α-amino glyoxals are readily accessible by oxidation of α-diazoketones derived from natural amino acids and dipeptides using dimethyldioxirane in acetone; the glyoxals can be trapped efficiently in reactions such as Wittig olefination and condensation with amines and vicinal diamines.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1222-1223

Oxidation of α-diazoketones derived from L-amino acids and dipeptides using dimethyldioxirane. Synthesis and reactions of homochiral N-protected α-amino glyoxals

P. Darkins, N. McCarthy, M. A. McKervey and T. Ye, J. Chem. Soc., Chem. Commun., 1993, 1222 DOI: 10.1039/C39930001222

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