Issue 17, 1994
From the journal:

Journal of the Chemical Society, Chemical Communications

A route to dipeptides containing β-amino-α-hydroxy acid fragments by coupling of N-boc-β-lactams with α-amino esters. Application to the synthesis of (–)-bestatin

Claudio Palomo,   Jesús M Aizpurua  and  Carmen Cuevas  

Abstract

α-Amino esters are smoothly acylated by N-Boc-3-alkoxy-4-alkyl-β-lactams in DMF under the influence of sodium azide, giving a novel dipeptide coupling reaction.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39940001957
Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1957-1958

Permissions

Request permissions

A route to dipeptides containing β-amino-α-hydroxy acid fragments by coupling of N-boc-β-lactams with α-amino esters. Application to the synthesis of (–)-bestatin

C. Palomo, J. M. Aizpurua and C. Cuevas, J. Chem. Soc., Chem. Commun., 1994, 1957 DOI: 10.1039/C39940001957

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