Issue 10, 2015

Base-promoted cascade reaction of isocyanides, selenium and amines: a practical approach to 2-aminobenzo[d][1,3]selenazines under metal-free conditions

Abstract

A new practical approach for constructing 2-aminobenzo[d][1,3]selenazines by base mediated multicomponent reaction of isocyanides, selenium and amines under metal-free conditions is reported. A series of selenazine derivatives are observed in moderate to excellent yields.

Graphical abstract: Base-promoted cascade reaction of isocyanides, selenium and amines: a practical approach to 2-aminobenzo[d][1,3]selenazines under metal-free conditions

Supplementary files

Article information

Article type
Research Article
Submitted
06 May 2015
Accepted
27 Jul 2015
First published
28 Jul 2015

Org. Chem. Front., 2015,2, 1338-1341

Base-promoted cascade reaction of isocyanides, selenium and amines: a practical approach to 2-aminobenzo[d][1,3]selenazines under metal-free conditions

Y. Fang, S. Wang, X. Shen and S. Ji, Org. Chem. Front., 2015, 2, 1338 DOI: 10.1039/C5QO00150A

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