A Toolbox of Reagents for Trifluoromethylthiolation: From Serendipitous Findings to Rational Design-Reference-Cited by-同舟云学术

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A Toolbox of Reagents for Trifluoromethylthiolation: From Serendipitous Findings to Rational Design

Published:2023-02-16 Issue:6 Volume:88 Page:3359-3371
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shen Qilong¹^ORCID

Affiliation:

1. Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Shanghai institute of Organic Chemistry

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02777

Reference116 articles.

1. Partition coefficients and their uses

2. A survey of Hammett substituent constants and resonance and field parameters

3. Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept

4. Shelf-Stable Electrophilic Reagents for Trifluoromethylthiolation

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

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2. Electrochemical Trifluoromethylthiolation/Cyclization of N-Arylacrylamides with AgSCF₃: Access to SCF₃-Containing Oxindoles;The Journal of Organic Chemistry;2024-08-19

3. Fluorinating electrophilic interception in the oxidation or protonation of alkynyl tetracoordinate borons;Chem;2024-08

4. Photocatalytic Perfluoroalkylation of Disulfides and Diselenides. Syntheses of Perfluoroalkyl Thio- and Seleno-ethers;The Journal of Organic Chemistry;2024-07-22

5. Transition-Metal-Free C–H Trifluoromethylthiolation of N,N-Disubstituted Enaminones To Access CF₃S-Functionalized Enaminones and Their Application in the Synthesis of CF₃S-Heteroaryls;The Journal of Organic Chemistry;2024-06-03

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