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