Issue 21, 2002
From the journal:

Chemical Communications

Extension of ring closing metathesis methodology to the synthesis of carbocyclic methyl and silyl enol ethers†

Varinder K. Aggarwal*a  and  Adrian M. Dalya  

* Corresponding authors

a School of Chemistry, University of Bristol, Cantock’s Close, Bristol, UK
E-mail: v.aggarwal@bristol.ac.uk
Fax: +44-117-9298611
Tel: +44-117-9546315

Abstract

Carbocyclic methyl and silyl enol ethers (TBDMS is optimum) can be synthesised regiospecifically by ring closing metathesis using the ‘second generation’ Grubbs ruthenium carbene catalyst in combination with molecular sieves.

Graphical abstract: Extension of ring closing metathesis methodology to the synthesis of carbocyclic methyl and silyl enol ethers

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Article information

DOI
https://doi.org/10.1039/B208445G
Article type
Communication
Submitted
30 Aug 2002
Accepted
26 Sep 2002
First published
09 Oct 2002

Chem. Commun., 2002, 2490-2491

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Extension of ring closing metathesis methodology to the synthesis of carbocyclic methyl and silyl enol ethers

V. K. Aggarwal and A. M. Daly, Chem. Commun., 2002, 2490 DOI: 10.1039/B208445G

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