Issue 72, 2018

Reductive cyclisations of amidines involving aminal radicals

Abstract

Amidines bearing simple alkenes undergo aminal radical cyclisation upon treatment with SmI2. The mild, reductive electron transfer process delivers medicinally-relevant, polycyclic quinazolinone derivatives in good to excellent yield and typically with complete diastereocontrol.

Graphical abstract: Reductive cyclisations of amidines involving aminal radicals

Supplementary files

Article information

Article type
Communication
Submitted
28 জুন 2018
Accepted
14 আগ. 2018
First published
15 আগ. 2018

Chem. Commun., 2018,54, 10160-10163

Reductive cyclisations of amidines involving aminal radicals

H. Huang, R. W. Adams and D. J. Procter, Chem. Commun., 2018, 54, 10160 DOI: 10.1039/C8CC05178J

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