Issue 3, 2000

The synthesis of novel heterocyclic substituted α-amino acids; further exploitation of α-amino acid alkynyl ketones

Abstract

A range of novel heterocyclic substituted α-amino acids has been synthesised by cyclocondensations of (S)-2-tert-butoxycarbonylamino-4-oxohex-5-ynoic acid tert-butyl ester with enamines, phenylhydrazine, hydroxylamine and phenyl azide.

Article information

Article type
Communication
Submitted
09 Dec 1999
Accepted
21 Dec 1999
First published
25 Jan 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 303-305

The synthesis of novel heterocyclic substituted α-amino acids; further exploitation of α-amino acid alkynyl ketones

R. M. Adlington, J. E. Baldwin, D. Catterick, G. J. Pritchard and L. T. Tang, J. Chem. Soc., Perkin Trans. 1, 2000, 303 DOI: 10.1039/A909720A

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