Issue 10, 2001

Conversion of homochiral amines, β-amino alcohols and α-amino acids to their chiral 2-substituted pyrrole derivatives

Abstract

The conversion of the amino group of chiral amines, amino alcohols, amino acids and their esters into chiral 2-substituted pyrrole derivatives with various halogeno enones is described. The conversion works in good yield and without racemization. The synthesis of 2-phenylpyrrole derivatives was possible with amino alcohols but not with amino acids or their esters.

Graphical abstract: Conversion of homochiral amines, β-amino alcohols and α-amino acids to their chiral 2-substituted pyrrole derivatives

Article information

Article type
Paper
Submitted
16 Oct 2000
Accepted
22 Mar 2001
First published
24 Apr 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 1162-1167

Conversion of homochiral amines, β-amino alcohols and α-amino acids to their chiral 2-substituted pyrrole derivatives

A. S. Demir, İ. M. Akhmedov, Ö. Şeşenoǧlu, O. Alptürk, S. Apaydın, Z. Gerçek and N. İbrahimzade, J. Chem. Soc., Perkin Trans. 1, 2001, 1162 DOI: 10.1039/B008317H

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