Inversion versus Retention of Configuration for Nucleophilic Substitution at Vinylic Carbon-Reference-Cited by-同舟云学术

Inversion versus Retention of Configuration for Nucleophilic Substitution at Vinylic Carbon

Published:2001-05-24 Issue:24 Volume:123 Page:5787-5793
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bach Robert D.¹,Baboul Anwar G.¹,Schlegel H. Bernhard¹

Affiliation:

1. Contribution from the Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, Division of Chemistry, Argonne National Laboratory, Argonne Illinois 60439, and Department of Chemistry, Wayne State University, Detroit, Michigan 48202

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja010234y

Reference54 articles.

1. The rapid steps in nucleophilic vinylic addition-elimination substitution. Recent developments

2. The rich mechanistic world of nucleophilic vinylic (SN V) substitution

3. Nucleophilic vinylic substitution. A single- or a multi-step process?

4. Nucleophilic attacks on carbon-carbon double bonds. 28. Complete and partial stereoconversion in the substitution of methyl (E)- and (Z)-.beta.-chloro-.alpha.-cyano-p-nitrocinnamates by nucleophiles

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