Nonbasic Synthesis of Thioethers via Nickel-Catalyzed Reductive Thiolation Utilizing NBS-Like N-Thioimides as Electrophilic Sulfur Donors
Author:
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
Funder
National Natural Science Foundation of China
Hangzhou Leading Innovation and Entrepreneurship Team Project
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02360
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3. Design and synthesis of ether analogues as potent and selective M2 muscarinic receptor antagonists
4. Enzymatic Carbon–Sulfur Bond Formation in Natural Product Biosynthesis
5. Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry
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1. Correction to “Nonbasic Synthesis of Thioethers via Nickel-Catalyzed Reductive Thiolation Utilizing NBS-Like N-Thioimides as Electrophilic Sulfur Donors”;The Journal of Organic Chemistry;2024-08-15
2. Copper-Catalyzed Chemoselective Coupling of N-Dithiophthalimides and Alkyl Halides: Synthesis of Unsymmetrical Disulfides and Sulfides;Organic Letters;2024-04-25
3. Selective nickel-catalyzed disulfuration of alkyl halides with di/trithiosulfonates;Organic Chemistry Frontiers;2024
4. Sodium Halides-Promoted S—Si Bond Activation and Its Application in the Synthesis of Unsymmetrical Thioethers;Chinese Journal of Organic Chemistry;2024
5. Research Progress in C—S Coupling Reactions of Aryl Halides;Chinese Journal of Organic Chemistry;2023
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