Issue 18, 1997
From the journal:

Chemical Communications

Highly diastereoselective radical addition to glyoxylic oxime ether: asymmetric synthesis of α-amino acids

Hideto Miyabe,   Chikage Ushiro  and  Takeaki Naito  

Abstract

A high degree of stereocontrol in radical addition to the Oppolzer’s camphor sultam derivative of glyoxylic oxime ether was achieved, providing a convenient method for preparing a variety of enantiomerically pure α-amino acids.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/A704562J
Article type
Paper

Chem. Commun., 1997, 1789-1790

Permissions

Request permissions

Highly diastereoselective radical addition to glyoxylic oxime ether: asymmetric synthesis of α-amino acids

H. Miyabe, C. Ushiro and T. Naito, Chem. Commun., 1997, 1789 DOI: 10.1039/A704562J

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.

Social activity

Spotlight

Advertisements