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Stereoselective Alkene Synthesis

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Attention for Chapter 314: Olefination Reactions of Phosphorus-Stabilized Carbon Nucleophiles
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Chapter title
Olefination Reactions of Phosphorus-Stabilized Carbon Nucleophiles
Chapter number 314
Book title
Stereoselective Alkene Synthesis
Published in
Topics in current chemistry, February 2016
DOI 10.1007/128_2012_314
Pubmed ID
Book ISBNs
978-3-64-231823-8, 978-3-64-231824-5
Authors

Yonghong Gu, Shi-Kai Tian, Gu, Yonghong, Tian, Shi-Kai

Abstract

A range of phosphorus-stabilized carbon nucleophiles have been employed for alkene synthesis with high chemo-, regio-, and stereoselectivity. The Wittig, Horner-Wadsworth-Emmons, Horner-Wittig, and Evans-Akiba reactions utilize phosphonium-, phosphonate-, phosphine oxide-, and pentacoordinated phosphorane-stabilized carbanions as nucleophiles, respectively, to undergo olefination with aldehydes or ketones, and each of these transformations has its own advantages and limitations. Modifying the structures of these nucleophiles along with optimizing reaction conditions results in the formation of a wide variety of polysubstituted alkenes in a highly stereoselective manner. The olefination of imines with phosphonium ylides has recently emerged as a useful approach to tune the stereoselectivity for alkene synthesis. This review focuses on recent advances in the stereoselective olefination of phosphorus-stabilized carbon nucleophiles.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 20%
Student > Bachelor 2 20%
Professor > Associate Professor 1 10%
Student > Doctoral Student 1 10%
Unknown 4 40%
Readers by discipline Count As %
Chemistry 6 60%
Unknown 4 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 23 July 2014.
All research outputs
#20,233,066
of 22,758,963 outputs
Outputs from Topics in current chemistry
#129
of 147 outputs
Outputs of similar age
#336,780
of 400,275 outputs
Outputs of similar age from Topics in current chemistry
#10
of 11 outputs
Altmetric has tracked 22,758,963 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 147 research outputs from this source. They receive a mean Attention Score of 4.1. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 400,275 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 11 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.