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Two-directional cross-metathesis

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2009 English Publisher:Royal Society of Chemistry (RSC)Journal:Organic & Biomolecular Chemistry, volume 7, page 2,274 (issn: 1477-0520, eissn: 1477-0539, Copyright policy )
Authors: Annabella F, Newton; Stephen J, Roe; Jean-Christophe, Legeay; Pooja, Aggarwal; Camille, Gignoux; Nicola J, Birch; Robert, Nixon; +2 Authors

doi: 10.1039/b907720k

pmid: 19462035

Two-directional cross-metathesis

Abstract

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.

Related Organizations
Keywords

Alkadienes, Molecular Structure, Electrons, Stereoisomerism, Alkenes, Catalysis

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
15
Average
Top 10%
Top 10%
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