Issue 30, 2017

Pd-Catalyzed double N-arylation of primary amines to synthesize phenoxazines and phenothiazines

Abstract

An efficient and versatile Pd-catalyzed tandem C–N bond formation between aryl halides and primary amines is developed. The transformation allows a one-pot synthesis of phenoxazine and phenothiazine derivatives with a broad range of substitution patterns from readily available precursors.

Graphical abstract: Pd-Catalyzed double N-arylation of primary amines to synthesize phenoxazines and phenothiazines

Supplementary files

Article information

Article type
Communication
Submitted
25 Qas 2017
Accepted
07 Qad 2017
First published
07 Qad 2017

Org. Biomol. Chem., 2017,15, 6306-6309

Pd-Catalyzed double N-arylation of primary amines to synthesize phenoxazines and phenothiazines

L. Zhang, X. Huang, S. Zhen, J. Zhao, H. Li, B. Yuan and G. Yang, Org. Biomol. Chem., 2017, 15, 6306 DOI: 10.1039/C7OB01540B

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