New active heterogeneous olefin metathesis catalyst based on molybdenum oxotetrachloride
نویسندگان
چکیده
منابع مشابه
Diphenylamido Precursors to Bisalkoxide Molybdenum Olefin Metathesis Catalysts.
We have found that Mo(NAr)(CHR')(NPh(2))(2) (R' = t-Bu or CMe(2)Ph) and Mo(NAr')(CHCMe(2)Ph)(NPh(2))(2) (Ar = 2,6-i-Pr(2)C(6)H(3); Ar' = 2,6-Me(2)C(6)H(3)) can be prepared through addition of two equivalents of LiNPh(2) to Mo(NR″)(CHR')(OTf)(2)(dme) species (R″ = Ar or Ar' dme = 1,2-dimethoxyethane), although yields are low. A high yield route consists of addition of LiNPh(2) to bishexafluro-t-...
متن کاملSynthesis of Molybdenum Olefin Metathesis Catalysts through Protonation Reactions
Chapter 1 The attempted syntheses of molybdenum imido alkylidene complexes of the type Mo(NArc,)(CH-t-Bu)[Biphen] and Mo(N-2-CF 3C6H4)(CHCMe 2Ph)[Biphen] (Biphen2 = 3,3'-di-t-butyl-5,5',6,6'-tetramethyl1,1'-biphenyl-2,2'-diolate) from Mo(NArcl)(CH-tBu)(OTf)2(dme) and [Biphen]K2 have sporadically afforded mixtures containing the desired products along with the corresponding amido alkylidyne comp...
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Olefin metathesis as a catalytic process constantly gains interest among organic chemists. Over the last decade, it became an efficient tool to accomplish the synthesis of many complex molecules. The development of new well-defined catalysts and continuous examination of novel ligands led to the establishment of metathesis methodology in a group of widespread chemical transformations. Not only ...
متن کاملAllyl 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.
متن کاملLow catalyst loadings in olefin metathesis: synthesis of nitrogen heterocycles by ring-closing metathesis.
A series of ruthenium catalysts have been screened under ring-closing metathesis (RCM) conditions to produce five-, six-, and seven-membered carbamate-protected cyclic amines. Many of these catalysts demonstrated excellent RCM activity and yields with as low as 500 ppm catalyst loadings. RCM of the five-membered carbamate series could be run neat, the six-membered carbamate series could be run ...
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ژورنال
عنوان ژورنال: Kinetics and Catalysis
سال: 2010
ISSN: 0023-1584,1608-3210
DOI: 10.1134/s0023158410040233