Two-directional cross-metathesis
Two-directional cross-metathesis of a range of alpha,omega dienes with a variety of electron deficient alkenes has been accomplished. It was found that the process is quite general and gives complete selectivity for the E,E-dienes, making this a very useful and high yielding protocol for two-directi...
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Veröffentlicht in: | Organic & biomolecular chemistry 2009-01, Vol.7 (11), p.2274-2277 |
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container_title | Organic & biomolecular chemistry |
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creator | Newton, Annabella F Roe, Stephen J Legeay, Jean-Christophe Aggarwal, Pooja Gignoux, Camille Birch, Nicola J Nixon, Robert Alcaraz, Marie-Lyne Stockman, Robert A |
description | Two-directional cross-metathesis of a range of alpha,omega dienes with a variety of electron deficient alkenes has been accomplished. It was found that the process is quite general and gives complete selectivity for the E,E-dienes, making this a very useful and high yielding protocol for two-directional chain elongation. |
doi_str_mv | 10.1039/b907720k |
format | Article |
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source | MEDLINE; Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
subjects | Alkadienes - chemical synthesis Alkadienes - chemistry Alkenes - chemical synthesis Alkenes - chemistry Catalysis Electrons Molecular Structure Stereoisomerism |
title | Two-directional cross-metathesis |
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