Synthesis of Unsymmetric Thiosulfonates Starting from N-Substituted <i>O</i>-Thiocarbamates: Easy Access to the S–SO<sub>2</sub> Bond-Reference-Cited by-同舟云学术

Synthesis of Unsymmetric Thiosulfonates Starting from N-Substituted O-Thiocarbamates: Easy Access to the S–SO₂ Bond

Published:2022-08-12 Issue:17 Volume:87 Page:11656-11668
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yang Cheng-Li¹,Gao Xue-Jie¹,Jiang Xin-Yi¹,Shi Zhen²,Hao Er-Jun³,Dong Zhi-Bing¹²³⁴⁵^ORCID

Affiliation:

1. School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China

2. Hubei Key Laboratory of Biologic Resources Protection and Utilization, Hubei Minzu University, Enshi 445000, China

3. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China

4. Key Laboratory of Green Chemical Process, Ministry of Education, Wuhan Institute of Technology, Wuhan 430205, China

5. Engineering Research Center of Phosphorus Resources Development and Utilization, Ministry of Education, Wuhan Institute of Technology, Wuhan 430205, China

Funder

Wuhan Institute of Technology

Henan Normal University

State Key Laboratory of Environmental Chemistry and Ecotoxicology

Hubei Key Laboratory of Biologic Resources Protection and Utilization, Hubei Minzu University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01301

Reference59 articles.

1. Good Partnership between Sulfur and Fluorine: Sulfur-Based Fluorination and Fluoroalkylation Reagents for Organic Synthesis

2. A cysteine residue in the third membrane-spanning segment of the human D2 dopamine receptor is exposed in the binding-site crevice.

3. Stimulation of Topoisomerase II-Mediated DNA Damage via a Mechanism Involving Protein Thiolation

4. Recent Developments in the Synthesis and Utilization of Chiral Sulfoxides

5. Alkyl and Aryl Thiolsulfonates

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