Issue 20, 2000
From the journal:

Chemical Communications

The first vanadium-catalyzed oxidation of aryl allylic selenides with in situ [2,3] sigmatropic rearrangementElectronic supplementary information (ESI) available: typical experimental procedure for synthesis of 1–6. See http://www.rsc.org/suppdata/cc/b0/b006278m/

Rich G. Carter*a  and  T. Campbell Bourlanda  

* Corresponding authors

a Department of Chemistry and Biochemistry, University of Mississippi, Oxford, USA.
E-mail: rgcarter@olemiss.edu

Abstract

The efficient synthesis of a series of 2° allylic alcohols from a vanadium-catalyzed oxidation of suitably disposed allylic selenides with tandem [2,3] sigmatropic rearrangement is outlined.

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Article information

DOI
https://doi.org/10.1039/B006278M
Article type
Communication
Submitted
28 Jul 2000
Accepted
01 Sep 2000
First published
28 Sep 2000

Chem. Commun., 2000, 2031-2032

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The first vanadium-catalyzed oxidation of aryl allylic selenides with in situ [2,3] sigmatropic rearrangement

R. G. Carter and T. C. Bourland, Chem. Commun., 2000, 2031 DOI: 10.1039/B006278M

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