Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 39, Pages 13594-13595Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja106365j
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- Deutsche Forschungsgemeinschaft
- Fonds der Chemischen Industrie
- Alexander von Humboldt Foundation
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Internal alkynes undergo 1,1-carboboration reactions upon treatment with boranes RB(C(6)F(5))(2) (R = C(6)F(5), CH(3)) to yield trisubstituted alkenylboranes. These products can be used as substrates in Pd-catalyzed cross-coupling reactions.
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