Issue 11, 2000
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Stereoselectivity in the synthesis of conformationally constrained vicinally dihydroxylated cyclic α-amino acids

Kristin Hammer,a   Jing Wang,a   Mette Lene Falck-Pedersen,a   Christian Rømminga  and  Kjell Undheim*a  

* Corresponding authors

a Department of Chemistry, University of Oslo, Oslo, Norway

Abstract

Stereoselective syntheses of precursors to vicinal cis-dihydroxy-1-aminocyclopentane- and -cyclohexane-carboxylic acid methyl esters and their methoxy analogues are described. The chiral products are isolated as pure enantiomers. The absolute configurations at the new stereogenic centres are established by X-ray analysis.

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B001779P
Article type
Paper
Submitted
06 Mar 2000
Accepted
27 Mar 2000
First published
05 May 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 1691-1695

Permissions

Request permissions

Stereoselectivity in the synthesis of conformationally constrained vicinally dihydroxylated cyclic α-amino acids

K. Hammer, J. Wang, M. L. Falck-Pedersen, C. Rømming and K. Undheim, J. Chem. Soc., Perkin Trans. 1, 2000, 1691 DOI: 10.1039/B001779P

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