Issue 3, 2004
From the journal:

Chemical Communications

A versatile and concise route to carbocycles using a 1,6-electrocyclic reaction†

Svante Brandänge*a  and  Hans Leijonmarcka  

* Corresponding authors

a Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden
E-mail: svante@organ.su.se
Fax: +46 8 15 49 08
Tel: +46 8 16 24 84

Abstract

The viability of the 1,6-electrocyclic route to 1,3-cyclohexadienes has been significantly increased by using a phenylsulfonyl substituent in a multi-purpose (≥3) role.

Graphical abstract: A versatile and concise route to carbocycles using a 1,6-electrocyclic reaction

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Article information

DOI
https://doi.org/10.1039/B311815K
Article type
Communication
Submitted
26 Sep 2003
Accepted
21 Nov 2003
First published
18 Dec 2003

Chem. Commun., 2004, 292-293

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A versatile and concise route to carbocycles using a 1,6-electrocyclic reaction

S. Brandänge and H. Leijonmarck, Chem. Commun., 2004, 292 DOI: 10.1039/B311815K

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