Synthesis of α-Bromo Arylethyl Sulfonyl Fluorides and β-Arylethenesulfonyl Fluorides via Copper-Catalyzed Meerwein Arylation-Reference-Cited by-同舟云学术

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Synthesis of α-Bromo Arylethyl Sulfonyl Fluorides and β-Arylethenesulfonyl Fluorides via Copper-Catalyzed Meerwein Arylation

Published:2024-08-16 Issue: Volume: Page:
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Ming-Jian¹,Fayad Eman²^ORCID,Abu Ali Ola A.³,Tao Xiang-Feng⁴,Qin Hua-Li¹^ORCID

Affiliation:

1. State Key Laboratory of Silicate Materials for Architectures and School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan 430070, People’s Republic of China

2. Department of Biotechnology, College of Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia

3. Department of Chemistry, College of Science, Taif University, Taif 21944, Saudi Arabia

4. School of Chemistry, Chemical Engineering and Life Sciences,Sciences, Wuhan University of Technology, Wuhan 430070, People’s Republic of China

Funder

Taif University

Wuhan University of Technology

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01002

Reference50 articles.

1. Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry

2. Multidimensional SuFEx Click Chemistry: Sequential Sulfur(VI) Fluoride Exchange Connections of Diverse Modules Launched From An SOF4 Hub

3. Click Chemistry: Evolving on the Fringe

4. The growing applications of SuFEx click chemistry

5. Metal‐Free Synthesis of Functional 1‐Substituted‐1,2,3‐Triazoles from Ethenesulfonyl Fluoride and Organic Azides

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