Issue 16, 2015
From the journal:

Organic & Biomolecular Chemistry

Palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines with isocyanides through double sp2 C–H bonds cleavage: facile synthesis of 4-aminoquinoline derivatives†

Qiang Zheng,a   Puying Luo,*b   Yuqing Lin,a   Wenfan Chen,a   Xiuxiu Liu,a   Yadong Zhanga  and  Qiuping Ding*a  

* Corresponding authors

a Key Laboratory of Functional Small Organic Molecules, Ministry of Education and College of Chemistry & Chemical Engineering, Jiangxi Normal University, Nanchang, Jiangxi 330022, P. R. China
E-mail: dqpjxnu@gmail.com
Fax: +86 791 88120380
Tel: +86 791 88120380

b Department of Obstetrics and Gynecology, Jiangxi Provincial people's Hospital, Nanchang, Jiangxi 330006, P. R. China
E-mail: luopuying1979@gmail.com

Abstract

An efficient method for the synthesis of 4-aminoquinolines via palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines and isocyanides through double sp2 C–H bonds cleavage has been developed.

Graphical abstract: Palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines with isocyanides through double sp2 C–H bonds cleavage: facile synthesis of 4-aminoquinoline derivatives

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C5OB00329F
Article type
Communication
Submitted
16 Feb 2015
Accepted
11 Mar 2015
First published
11 Mar 2015

Org. Biomol. Chem., 2015,13, 4657-4660

Author version available

Download author version (PDF)

Permissions

Request permissions

Palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines with isocyanides through double sp2 C–H bonds cleavage: facile synthesis of 4-aminoquinoline derivatives

Q. Zheng, P. Luo, Y. Lin, W. Chen, X. Liu, Y. Zhang and Q. Ding, Org. Biomol. Chem., 2015, 13, 4657 DOI: 10.1039/C5OB00329F

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