Issue 61, 2014

Pd-Catalyzed C–H activation/oxidative cyclization of acetanilide with norbornene: concise access to functionalized indolines

Abstract

An efficient Pd-catalyzed oxidative cyclization reaction for the synthesis of functionalized indolines by direct C–H activation of acetanilide has been developed. The norbornylpalladium species formed via direct ortho C–H activation of acetanilides is supposed to be a key intermediate in this transformation.

Graphical abstract: Pd-Catalyzed C–H activation/oxidative cyclization of acetanilide with norbornene: concise access to functionalized indolines

Supplementary files

Article information

Article type
Communication
Submitted
24 Apr 2014
Accepted
02 Jun 2014
First published
18 Jun 2014

Chem. Commun., 2014,50, 8370-8373

Pd-Catalyzed C–H activation/oxidative cyclization of acetanilide with norbornene: concise access to functionalized indolines

Y. Gao, Y. Huang, W. Wu, K. Huang and H. Jiang, Chem. Commun., 2014, 50, 8370 DOI: 10.1039/C4CC03062A

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