S‐Trifluoroethyl Benzenesulfonothioate: A Bench‐Stable Reagent for Electrophilic Trifluoroethylthiolation †-Reference-Cited by-同舟云学术

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S‐Trifluoroethyl Benzenesulfonothioate: A Bench‐Stable Reagent for Electrophilic Trifluoroethylthiolation †

Published:2020-10-07 Issue:12 Volume:38 Page:1625-1628
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Huang Shuai¹,Xia Ziheng¹,Lu Kui²,Lu Haifeng¹,Tung Chen‐Ho¹,Xu Zhenghu¹³

Affiliation:

1. Key Lab for Colloid and Interface Chemistry of Education Ministry, Shandong University Jinan Shandong 250100 China

2. Land Surveying and Mapping Institute of Shandong Province Jinan Shandong 250013 China

3. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences Shanghai 200032 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202000279

Reference53 articles.

1. For reviews see: (a) O'Hagan D. Understanding Organofluorine Chemistry. An Introduction to the C‐F Bond.Chem. Soc. Rev.2008 37 308−319;

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

3. Synthetic Methods for Compounds Having CF3–S Units on Carbon by Trifluoromethylation, Trifluoromethylthiolation, Triflylation, and Related Reactions

4. Preparation and Utility of Organic Pentafluorosulfanyl-Containing Compounds

5. Transition-Metal (Cu, Pd, Ni)-Catalyzed Difluoroalkylation via Cross-Coupling with Difluoroalkyl Halides

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3. Bench‐Stable Electrophilic Reagents for the Direct Di‐ and Trifluoroethylthiolation of Indoles;Advanced Synthesis & Catalysis;2023-07-06

4. Synthesis and applications of thiosulfonates and selenosulfonates as free-radical reagents;Chinese Chemical Letters;2023-04

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