Radical selenation of C(sp<sup>3</sup>)–H bonds to asymmetric selenides and mechanistic study-Reference-Cited by-同舟云学术

Radical selenation of C(sp³)–H bonds to asymmetric selenides and mechanistic study

Published:2022 Issue:10 Volume:58 Page:1526-1529
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wang Xin¹,Lei Jia¹,Guo Sa¹,Zhang Yan¹,Ye Yong²,Tang Shi³^ORCID,Sun Kai¹^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Yantai University, Yantai, 264005, Shandong, P. R. China

2. College of Chemistry, Zhengzhou University, Zhengzhou, 450001, P. R. China

3. College of Chemistry and Chemical Engineering, Jishou University, Jishou, 416000, China

Abstract

Herein, the oxidative radical selenation of C(sp3)–H bonds to asymmetric selenides was developed. Various C(sp3)–H bonds with ethers, thioethers, and toluene derivatives were found to be suitable substrates for this novel transformation.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D1CC06323E

Reference69 articles.

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2. Synthesis of Vinyl Selenides

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4. Selenium-Containing Fused Bicyclic Heterocycle Diselenolodiselenole: Field Effect Transistor Study and Structure–Property Relationship

5. Chemistry of Biologically Important Synthetic Organoselenium Compounds

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