Issue 1, 2000

Kinetic resolution of amines by acylation using3-diacylaminoquinazolin-4(3H)-ones

Abstract

Four diastereoisomeric 3-diacylaminoquinazolinones 8a–d have been separated and identified by X-ray structure determinations on three of them: their stoichiometric reactions with α-phenylethylamine and with 2-methylpiperidine (2 equiv. of amine) gave the corresponding N-(2-acetoxypropanoyl)amine and unreacted amine in high diastereomeric/enantiomeric excess.

Supplementary files

Article information

Article type
Communication
Submitted
04 Oct 1999
Accepted
16 Nov 1999
First published
24 Dec 1999

Chem. Commun., 2000, 43-44

Kinetic resolution of amines by acylation using

3-diacylaminoquinazolin-4(3H)-ones

A. G. Al-Sehemi, R. S. Atkinson, J. Fawcett and D. R. Russell, Chem. Commun., 2000, 43 DOI: 10.1039/A907970J

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