Issue 3, 2001
From the journal:

Chemical Communications

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

Peter J. J. A. Buijnsters,ab   Martinus C. Feiters,a   Roeland J. M. Nolte,ac   Nico A. J. M. Sommerdijk*ac  and  Binne Zwanenburga  

* Corresponding authors

a Department of Organic Chemistry, NSR Centre, University of Nijmegen, Toernooiveld NL-6525 ED Nijmegen, The Netherlands.
E-mail: N.Sommerdijk@tue.nl

b Department of Medicinal Chemistry, Janssen Research Foundation, Beerse, Belgium

c Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, Eindhoven, The Netherlands

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.

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Article information

DOI
https://doi.org/10.1039/B009294K
Article type
Communication
Submitted
20 Nov 2000
Accepted
20 Dec 2000
First published
23 Jan 2001

Chem. Commun., 2001, 269-270

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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

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