Issue 11, 1986

Chiral aziridination of alkenes: oxidation of 3-amino-2-(1,2,2-trimethyl)propylquinazolin-4(3H)-one in the presence of alkenes

Abstract

Oxidation of the title N-aminoquinazolone (2) in dichloromethane in the presence of α-methylene-γ-butyrolactone gave a 1 : 1 : 3 ratio of stereoisomers (3): if the oxidation is carried out in the presence of a small quantity of trifluoroacetic acid (TFA), only one of these stereoisomers in produced in 72% yield.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 834-835

Chiral aziridination of alkenes: oxidation of 3-amino-2-(1,2,2-trimethyl)propylquinazolin-4(3H)-one in the presence of alkenes

R. S. Atkinson and G. Tughan, J. Chem. Soc., Chem. Commun., 1986, 834 DOI: 10.1039/C39860000834

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