Issue 21, 2003
From the journal:

Chemical Communications

Thermodynamically controlled cyclisation reactions with double phenylsulfanyl migration

Julie Carlisle,a   David J. Foxa  and  Stuart Warren*a  

* Corresponding authors

a University Chemical Laboratory, Lensfield Road, Cambridge, UK
E-mail: sw134@cam.ac.uk

Abstract

Enantiomerically enriched C2-symmetric tetrols were synthesised by a route involving a ‘self-metathesis’ reaction with Grubbs' second-generation ruthenium catalyst; these tetrols produced interesting bicyclic products when rearranged under acidic conditions.

Graphical abstract: Thermodynamically controlled cyclisation reactions with double phenylsulfanyl migration

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Article information

DOI
https://doi.org/10.1039/B308609G
Article type
Communication
Submitted
23 Jul 2003
Accepted
05 Sep 2003
First published
30 Sep 2003

Chem. Commun., 2003, 2696-2697

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Thermodynamically controlled cyclisation reactions with double phenylsulfanyl migration

J. Carlisle, D. J. Fox and S. Warren, Chem. Commun., 2003, 2696 DOI: 10.1039/B308609G

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