Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.

Org Lett

Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.

Published: August 2015

A copper-catalyzed formal [4 + 1] cycloaddition of benzamides and isonitriles via 8-aminoquinoline-directed C-H cleavage has been developed. The reaction proceeds well even in the presence of a base metal catalyst, CuBr·SMe2, alone to deliver the corresponding 3-iminoisoindolinones in good yields. Moreover, the unique acceleration effects of diphenyl sulfide are also disclosed.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.5b01986DOI Listing

Publication Analysis

Top Keywords

copper-catalyzed formal
8
formal cycloaddition
8
cycloaddition benzamides
8
benzamides isonitriles
8
c-h cleavage
8
isonitriles directed
4
directed c-h
4
cleavage copper-catalyzed
4
isonitriles 8-aminoquinoline-directed
4
8-aminoquinoline-directed c-h
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!