Carbon−Carbon Bond Activation by 1,1-Carboboration of Internal Alkynes
Internal alkynes undergo 1,1-carboboration reactions upon treatment with boranes RB(C6F5)2 (R = C6F5, CH3) to yield trisubstituted alkenylboranes. These products can be used as substrates in Pd-catalyzed cross-coupling reactions.
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Veröffentlicht in: | Journal of the American Chemical Society 2010-10, Vol.132 (39), p.13594-13595 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Internal alkynes undergo 1,1-carboboration reactions upon treatment with boranes RB(C6F5)2 (R = C6F5, CH3) to yield trisubstituted alkenylboranes. These products can be used as substrates in Pd-catalyzed cross-coupling reactions. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja106365j |