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

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Article information

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

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

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

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

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