Literature DB >> 25410944

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

Grant A Edwards1, Phillip A Culp, Justin M Chalker.   

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.

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Year:  2015        PMID: 25410944     DOI: 10.1039/c4cc07932a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Preparation of 1-Tosyloxy-4-Substituted-2-butenes Using Ag(I) Salts.

Authors:  Jeffrey S Stehouwer; Mark M Goodman
Journal:  Tetrahedron Lett       Date:  2015-07-22       Impact factor: 2.415

2.  Bidirectional Synthesis of the IJK Fragment of Ciguatoxin CTX3C by Sequential Double Ring-Closing Metathesis and Tsuji-Trost Allylation.

Authors:  Michael Popadynec; Helen Gibbard; J Stephen Clark
Journal:  Org Lett       Date:  2020-04-19       Impact factor: 6.005

  2 in total

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