Issue 15, 2018

Accessing benzooxadiazepines via formal [4 + 3] cycloadditions of aza-o-quinone methides with nitrones

Abstract

An unprecedented and efficient [4 + 3] cycloaddition of N-(ortho-chloromethyl)aryl amides with nitrones has been developed. This approach provides easy access to a series of seven-membered benzooxadiazepine derivatives in good to excellent yields (up to 99% yield) under mild reaction conditions.

Graphical abstract: Accessing benzooxadiazepines via formal [4 + 3] cycloadditions of aza-o-quinone methides with nitrones

Supplementary files

Article information

Article type
Communication
Submitted
24 Jan 2018
Accepted
22 Mar 2018
First published
23 Mar 2018

Org. Biomol. Chem., 2018,16, 2639-2642

Accessing benzooxadiazepines via formal [4 + 3] cycloadditions of aza-o-quinone methides with nitrones

Y. Zheng, L. Tu, L. Gao, R. Huang, T. Feng, H. Sun, W. Wang, Z. Li and J. Liu, Org. Biomol. Chem., 2018, 16, 2639 DOI: 10.1039/C8OB00201K

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