Issue 9, 1989

Synthesis of chiral piperazin-2-ones as model peptidomimetics

Abstract

The enantiospecific synthesis of (3S,6R)-6-ethoxycarbonyl-3-(p-hydroxybenzyl)piperazin-2-one (1) and (3S)-1-(ethoxycarbonylmethyl)-3-(p-hydroxybenzyl)piperazin-2-one (2) and their enantiomers is described. The chiral C-6 centre of (1) is generated by a regiospecific protonation of the enamide precursor.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 1687-1689

Synthesis of chiral piperazin-2-ones as model peptidomimetics

J. DiMaio and B. Belleau, J. Chem. Soc., Perkin Trans. 1, 1989, 1687 DOI: 10.1039/P19890001687

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