Issue 4, 1975

Formation under kinetic control of aziridine invertomers

Abstract

The reaction of the stereoisomeric nitronic esters (1) and (2) with benzoylacetylene is stereoselective; each isomer leads to different aziridines, and the reaction allows the synthesis under control of N-methoxy-aziridine invertomers.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 112-113

Formation under kinetic control of aziridine invertomers

R. Grée and R. Carrié, J. Chem. Soc., Chem. Commun., 1975, 112 DOI: 10.1039/C39750000112

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