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

Grant Edwards; Phillip Culp; Justin Chalker

doi:10.1039/c4cc07932a

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

Grant Edwards, Phillip Culp, Justin Chalker

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

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. This journal is

Original language	English
Pages (from-to)	515-518
Number of pages	4
Journal	Chemical Communications
Volume	51
Issue number	3
DOIs	https://doi.org/10.1039/c4cc07932a
Publication status	Published - 11 Jan 2015

Access to Document

10.1039/c4cc07932a

Cite this

@article{ffccdbf9318d4359b310bb49f7b8a836,

title = "Allyl sulphides in olefin metathesis: catalyst considerations and traceless promotion of ring-closing metathesis",

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. This journal is",

author = "Grant Edwards and Phillip Culp and Justin Chalker",

year = "2015",

month = jan,

day = "11",

doi = "10.1039/c4cc07932a",

language = "English",

volume = "51",

pages = "515--518",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "ChemComm Communication",

number = "3",

}

TY - JOUR

T1 - Allyl sulphides in olefin metathesis: catalyst considerations and traceless promotion of ring-closing metathesis

AU - Edwards, Grant

AU - Culp, Phillip

AU - Chalker, Justin

PY - 2015/1/11

Y1 - 2015/1/11

N2 - 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. This journal is

AB - 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. This journal is

UR - http://www.scopus.com/inward/record.url?scp=84918543014&partnerID=8YFLogxK

U2 - 10.1039/c4cc07932a

DO - 10.1039/c4cc07932a

M3 - Article

SN - 1359-7345

VL - 51

SP - 515

EP - 518

JO - Chemical Communications

JF - Chemical Communications

IS - 3

ER -

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

Abstract

Access to Document

Other files and links

Fingerprint

Cite this