Weakly Nucleophilic Conjugate Bases of Superacids as Powerful Nucleophiles in Vinylic Bimolecular Nucleophilic Substitutions of Simple β-Alkylvinyl(aryl)-λ3-bromanes-Reference-Cited by-同舟云学术

Weakly Nucleophilic Conjugate Bases of Superacids as Powerful Nucleophiles in Vinylic Bimolecular Nucleophilic Substitutions of Simple β-Alkylvinyl(aryl)-λ3-bromanes

Published:2011-02-22 Issue:10 Volume:133 Page:3342-3344
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ochiai Masahito¹,Okubo Takuji¹,Miyamoto Kazunori¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja200479p

Reference38 articles.

1. Reactions of nucleophiles with ethylenic substrates

2. Stereoselection in nucleophilic substitution at an sp2 carbon

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

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

5. Application of the extended Hueckel molecular orbital method to the properties of vinyl cations. Conformational energies of some 1-cyclopropylvinyl cations and a comparison of SN2 displacements at saturated and vinyl carbon

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