Issue 39, 2013
From the journal:

Chemical Communications

Schischkiniin support studies: synthetic access to 1,1′-bisindoles†‡

Christy Wanga  and  Jonathan Sperry*a  

* Corresponding authors

a School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, New Zealand
E-mail: j.sperry@auckland.ac.nz
Fax: +64 9 373 7422
Tel: +64 9 373 7599 ext 88269

Abstract

The first general synthetic approach to 1,1′-bisindoles is described. Two simultaneous, ambient temperature Mori–Ban reactions were used to effect bisindolization of several diallylated hydrazobenzenes with minimal cleavage of the N–N bond.

Graphical abstract: Schischkiniin support studies: synthetic access to 1,1′-bisindoles

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C2CC37241J
Article type
Communication
Submitted
04 Okt 2012
Accepted
26 Okt 2012
First published
26 Okt 2012

Chem. Commun., 2013,49, 4349-4351

Permissions

Request permissions

Schischkiniin support studies: synthetic access to 1,1′-bisindoles

C. Wang and J. Sperry, Chem. Commun., 2013, 49, 4349 DOI: 10.1039/C2CC37241J

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