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Allyl sulphides in olefin metathesis: catalyst considerations and traceless promotion of ring-closing metathesis.

Authors :
Edwards GA
Culp PA
Chalker JM
Source :
Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2015 Jan 11; Vol. 51 (3), pp. 515-8.
Publication Year :
2015

Abstract

Allyl sulphides are reactive substrates in ruthenium-catalysed olefin metathesis reactions, provided each substrate is matched with a suitable catalyst. A profile of catalyst activity is described, along with the first demonstration of allyl sulphides as traceless promoters in relayed ring-closing metathesis reactions.

Details

Language :
English
ISSN :
1364-548X
Volume :
51
Issue :
3
Database :
MEDLINE
Journal :
Chemical communications (Cambridge, England)
Publication Type :
Academic Journal
Accession number :
25410944
Full Text :
https://doi.org/10.1039/c4cc07932a