Difluoro-λ3-Bromane-Induced Oxidative Carbon−Carbon Bond-Forming Reactions: Ethanol as an Electrophilic Partner and Alkynes as Nucleophiles
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja801097c
Reference19 articles.
1. Alcohols as Electrophiles in CC Bond-Forming Reactions: The Hydrogen Autotransfer Process
2. Contributions to the chemistry of bromine trifluoride part 3. Electronic influences on the fluorine—aryl substitution reaction of bromine trifluoride with monosubstituted phenyltrifluorosilanes
3. Synthesis, Structure, and Reaction of 1-Alkynyl(aryl)-λ3-bromanes
4. Synthesis and Characterization of β-Haloalkenyl-λ3-bromanes: Stereoselective Markovnikov Addition of Difluoro(aryl)-λ3-bromane to Terminal Acetylenes
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