Journal
CHEMICAL COMMUNICATIONS
Volume 49, Issue 71, Pages 7809-7811Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc44434a
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Funding
- Ministry of Education, Culture, Sports, Science and Technology, Japan
- Funding Program for Next Generation World-Leading Researchers [GR025]
- Grants-in-Aid for Scientific Research [24105505] Funding Source: KAKEN
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Reactions of propargylic halides with trifluoromethyltrimethylsilane in the presence of a catalytic amount of copper(I) thiophene-2-carboxylate (CuTC) have been found to give the corresponding trifluoromethylated products in good to high yields with a high selectivity.
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