Issue 33, 2017

Efficient syntheses of 3-hydroxyimino-1-isoindolinones and 3-methylene-1-isoindolinones via Cu-promoted C–H activation–nitroalkylation–intramolecular cyclization tandem processes

Abstract

Efficient and selective syntheses of 3-hydroxyimino-1-isoindolinones and 3-methylene-1-isoindolinones were achieved via 8-aminoquinoline assisted Cu-promoted coupling of benzamides with nitroalkanes. The reaction was found to go through C–H activation, nitroalkylation followed by intramolecular cyclization. 3-Hydroxyimino-1-isoindolinones were obtained with nitromethane whereas 3-methylene-1-isoindolinones were produced with higher nitroalkanes.

Graphical abstract: Efficient syntheses of 3-hydroxyimino-1-isoindolinones and 3-methylene-1-isoindolinones via Cu-promoted C–H activation–nitroalkylation–intramolecular cyclization tandem processes

Supplementary files

Article information

Article type
Communication
Submitted
15 Feb 2017
Accepted
28 Mar 2017
First published
30 Mar 2017

Chem. Commun., 2017,53, 4597-4600

Efficient syntheses of 3-hydroxyimino-1-isoindolinones and 3-methylene-1-isoindolinones via Cu-promoted C–H activation–nitroalkylation–intramolecular cyclization tandem processes

L. Yu, H. Huang, X. Chen, L. Hu, Y. Yu and Z. Tan, Chem. Commun., 2017, 53, 4597 DOI: 10.1039/C7CC01097D

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