Alkynyl trifluoromethyl selenide synthesis via oxidative trifluoromethylselenolation of terminal alkynes
Literature Information
Publication Date
2015-03-30
DOI
10.1039/C5QO00045A
Impact Factor
5.281
Authors
Yuguang Wang, Yi You, Zhiqiang Weng
View Original
Abstract
The synthesis of alkynyl trifluoromethyl selenides by Cu-mediated oxidative trifluoromethylselenolation of terminal alkynes is reported. Treatment of [(bpy)Cu(SeCF3)]2 with various terminal alkynes in the presence of an oxidant, Dess–Martin periodinane, led to the formation of trifluoromethylselenolated acetylenes bearing sensitive moieties such as alkoxy, halogens, trifluoromethyl, and heterocyclic groups.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
Recommended Compounds
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Heptadecanoic Acid 3-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-9-yl Ester
CAS Number:
1404053-62-8
Molecular Formula:
C40H59FN4O4
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3-[4-(difluoromethoxy)phenyl]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid
CAS Number:
1496564-27-2
Molecular Formula:
C25H21F2NO5
1-(5-Bromo-2-fluorophenyl)-2,2,2-trifluoroethanol
CAS Number:
1039827-16-1
Molecular Formula:
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