Issue 3, 2001

Autocatalytic ring opening of N-acylaziridines. Complete control over regioselectivity by orientation at interfaces

Abstract

Ring opening of 1-alkanoyl-2-phenoxymethylaziridines by phosphate ions yielding self-assembling phospholipid analogues proceeds in an autocatalytic fashion and with complete regioselectivity at an organic–aqueous interface.

Article information

Article type
Communication
Submitted
20 Nov 2000
Accepted
20 Dec 2000
First published
23 Jan 2001

Chem. Commun., 2001, 269-270

Autocatalytic ring opening of N-acylaziridines. Complete control over regioselectivity by orientation at interfaces

P. J. J. A. Buijnsters, M. C. Feiters, R. J. M. Nolte, N. A. J. M. Sommerdijk and B. Zwanenburg, Chem. Commun., 2001, 269 DOI: 10.1039/B009294K

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