Issue 19, 2000

Synthesis of β-substituted alanines viaMichael addition of nucleophiles to dehydroalanine derivatives

Abstract

Several β-substituted alanines are synthesised in high yields by a Michael addition of nucleophiles to N-acyl-N-(tert-butoxycarbonyl)dehydroalanine methyl ester, using mild reaction conditions and simple work-up procedures. The same method can be applied to dipeptides containing dehydroalanine.

Article information

Article type
Paper
Submitted
26 Apr 2000
Accepted
10 Jul 2000
First published
13 Sep 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 3317-3324

Synthesis of β-substituted alanines via Michael addition of nucleophiles to dehydroalanine derivatives

P. M. T. Ferreira, H. L. S. Maia, L. S. Monteiro, J. Sacramento and J. Sebastião, J. Chem. Soc., Perkin Trans. 1, 2000, 3317 DOI: 10.1039/B003353G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements