Copper-catalyzed ring-opening trifluoromethylthiolation/trifluoromethylselenolation of cyclopropanols with TsSCF3orSe-(trifluoromethyl) 4-methoxybenzenesulfonoselenoate
Author:
Affiliation:
1. College of Chemistry, Tianjin Key Laboratory of Structure and Performance for Functional Molecules, Tianjin Normal University, Tianjin 300387, China
2. College of Biotechnology, Tianjin University of Science & Technology, Tianjin 300457, China
Abstract
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00228D
Reference46 articles.
1. The Electronic Nature of Fluorine-containing Substituents
2. Partition coefficients and their uses
3. A survey of Hammett substituent constants and resonance and field parameters
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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