Issue 31, 2014

Assembly of indenamine derivatives through in situ formed N-sulfonyliminium ion initiated cyclization

Abstract

An expedient route to structurally diverse indenamine derivatives through condensation of the readily accessible substituted cinnamylaldehydes and sulfonylamines under the catalysis of FeCl3 has been developed, featuring high efficiency in the generation of two bonds and one ring in a single-step and water as the only by-product.

Graphical abstract: Assembly of indenamine derivatives through in situ formed N-sulfonyliminium ion initiated cyclization

Supplementary files

Article information

Article type
Communication
Submitted
14 Jan 2014
Accepted
25 Feb 2014
First published
26 Feb 2014

Chem. Commun., 2014,50, 4119-4122

Author version available

Assembly of indenamine derivatives through in situ formed N-sulfonyliminium ion initiated cyclization

X. Fan, H. Lv, Y. Guan, H. Zhu, X. Cui and K. Guo, Chem. Commun., 2014, 50, 4119 DOI: 10.1039/C4CC00310A

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