Electrochemical Fluorination Functionalization of gem-Difluoroalkenes with CsF as a Fluorine Source: Access to Fluoroalkyl Building Blocks
Author:
Affiliation:
1. Department of Chemistry, Jinan University, Guangzhou 510632, China
Funder
Basic and Applied Basic Research Foundation of Guangdong Province
Jinan University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03901
Reference45 articles.
1. The Unique Role of Fluorine in the Design of Active Ingredients for Modern Crop Protection
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1. Dimethyl sulfoxide-mediated dibromination of gem-difluoroalkenes with hydrobromic acid as reagent;Journal of Fluorine Chemistry;2024-10
2. Streamlined Electrochemical Dihalogenation (F, Cl, and Br) of gem‐Difluoroalkenes Using Hydrogen Halides as Reagents;European Journal of Organic Chemistry;2024-07-22
3. Electrochemically Direct Fluorination Functionalization of Styrenes with Different Fluorine Source: Access to Fluoroalkyl Derivatives;The Journal of Organic Chemistry;2024-06-14
4. Dimethyl Sulfoxide-Mediated Dibromination of Gem-Difluoroalkenes with Hydrobromic Acid as Reagent;2024
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