“Thiol-free synthesized” and sustainable thiolating synthons for nickel-catalyzed reductive assembly of sulfides with high efficiency-Reference-Cited by-同舟云学术

“Thiol-free synthesized” and sustainable thiolating synthons for nickel-catalyzed reductive assembly of sulfides with high efficiency

Published:2022 Issue:23 Volume:9 Page:6490-6497
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Yong¹,Xu Yuenian¹,Zhang Yan¹,Gao Wen-Chao²^ORCID,Shao Xinxin¹^ORCID

Affiliation:

1. College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou 311121, Zhejiang, People's Republic of China

2. College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, People's Republic of China

Abstract

Unsymmetrical sulfides are widely found in the pharmaceutical industry, organic synthesis, and materials science.

Funder

Hangzhou Normal University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO01317G

Reference57 articles.

1. Enzymatic Carbon–Sulfur Bond Formation in Natural Product Biosynthesis

2. Construction of sulfur-containing moieties in the total synthesis of natural products

3. Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry

4. Recent Progress in the Sulfur-Containing Perfume & Flavors Construction

5. Catalytic, Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis

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