A highly regio- and stereoselective selenoxide elimination of 1,2-bis[4-(trimethylsilyl)phenylseleno]alkanes to give (E)-alkenyl selenoxides and its mechanistic study-Reference-Cited by-同舟云学术

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A highly regio- and stereoselective selenoxide elimination of 1,2-bis[4-(trimethylsilyl)phenylseleno]alkanes to give (E)-alkenyl selenoxides and its mechanistic study

Published:2016-02 Issue:2 Volume:1 Page:189-194
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Tarao Asami¹,Niki Aya¹,Komagawa Shinsuke²,Arimitsu Kenji¹,Uchimoto Hitomi¹,Kawasaki Ikuo¹,Yamaguchi Kentaro²,Nishide Kiyoharu¹

Affiliation:

1. School of Pharmacy and Pharmaceutical Sciences; Mukogawa Women's University; 11-68 Koshien Kyuban-cho Nishinomiya, Hyogo 663-8179 Japan

2. Pharmaceutical Sciences at Kagawa Campus; Tokushima Bunri University, 1314-1 Shido; Sanuki, Kagawa 769-2193 Japan

Publisher

Wiley

Subject

General Chemistry

Reference32 articles.

1. Organoselenium Chemistry: Synthesis and Reactions 2011

2. Organoselenium Chemistry in Stereoselective Reactions

3. Novel Reactions Using Organoselenium Compounds

4. Functional group manipulation using organoselenium reagents

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Oxidation and Reduction;Organic Reaction Mechanisms · 2016;2020-01-13

2. Selective Oxidation of Sulfides in Flow Chemistry;European Journal of Organic Chemistry;2018-05-11

3. ChemInform Abstract: A Highly Regio- and Stereoselective Selenoxide Elimination of 1,2-Bis[4-(trimethylsilyl)phenylseleno]alkanes to Give (E)-Alkenyl Selenoxides and Its Mechanistic Study.;ChemInform;2016-06

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