Issue 70, 2016

N-Hydroxyphthalimide: a new photoredox catalyst for [4+1] radical cyclization of N-methylanilines with isocyanides

Abstract

The first utilization of N-hydroxyphthalimide (NHPI) as an organophotoredox catalyst is demonstrated by the [4+1] radical cyclization reaction of N-methylanilines with isocyanides. The protocol offers an operationally simple one-pot synthesis of 3-iminodihydroindoles at room temperature.

Graphical abstract: N-Hydroxyphthalimide: a new photoredox catalyst for [4+1] radical cyclization of N-methylanilines with isocyanides

Supplementary files

Article information

Article type
Communication
Submitted
09 Jun 2016
Accepted
26 Jul 2016
First published
01 Aug 2016

Chem. Commun., 2016,52, 10621-10624

N-Hydroxyphthalimide: a new photoredox catalyst for [4+1] radical cyclization of N-methylanilines with isocyanides

A. K. Yadav and L. D. S. Yadav, Chem. Commun., 2016, 52, 10621 DOI: 10.1039/C6CC04846C

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