The M1 Phase of MoVTeNbO as a Catalyst for Olefin Metathesis and Isomerization

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Prevention of undesirable isomerization during olefin metathesis.

1,4-Benzoquinones have been found to prevent olefin isomerization of a number of allylic ethers and long-chain aliphatic alkenes during ruthenium-catalyzed olefin metathesis reactions. Electron-deficient benzoquinones are the most effective additives for the prevention of olefin migration. This mild, inexpensive, and effective method to block olefin isomerization increases the synthetic utility...

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A One-Pot Tandem Olefin Isomerization/Metathesis-Coupling (ISOMET) Reaction

A tandem catalytic reaction has been developed as part of a process to discover tungsten-based olefin metathesis catalysts that have a strong preference for terminal olefins over cis or trans internal isomers in olefin metathesis. This tandem isomerization/terminal olefin metathesis reaction (ISOMET) converts Cn trans internal olefins into C2n−2 cis olefins and ethylene. This reaction is made p...

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Olefin metathesis as a tool for multinuclear Co(III)salen catalyst construction: access to cooperative catalysts.

The construction of novel (macrocyclic) multinuclear Co(III)salen catalysts is reported. Olefin metathesis has been used as a key construction tool for the multimetallic structures starting from versatile allyl-substituted salen scaffolds. The Co(III) complexes were tested in the hydrolytic kinetic resolution of (rac)-1,2-epoxyhexane and epoxide ring opening reactions using methanol as the nucl...

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

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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ژورنال

عنوان ژورنال: ChemCatChem

سال: 2014

ISSN: 1867-3880

DOI: 10.1002/cctc.201402608