Catalytic C(sp)–Si cross-coupling silylation of alkynyl bromides with hydrosilanes by palladium catalysis
Transition metal-catalyzed silicon–carbon bond-forming silylation is one of the most important processes and remains an ongoing challenge in both organosilicon chemistry and homogeneous catalysis. Herein, we report an unprecedented and convenient Si–C(sp) bond-forming cross-coupling of alkynyl bromi...
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Veröffentlicht in: | Organic Chemistry Frontiers 2022-10, Vol.9 (21), p.5891-5898 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Transition metal-catalyzed silicon–carbon bond-forming silylation is one of the most important processes and remains an ongoing challenge in both organosilicon chemistry and homogeneous catalysis. Herein, we report an unprecedented and convenient Si–C(sp) bond-forming cross-coupling of alkynyl bromides with hydrosilanes, which provides highly chemoselective and facile access to the synthesis of alkynylsilanes and their derivatives in high yields. The catalytic C(sp)–Si cross-coupling is controlled by palladium/Xantphos catalyst systems, which demonstrates the powerful potential of this silylation for the preparation of structurally diverse alkynylsilanes, including the catalytic enantioselective synthesis of alkynylsilane with promising enantioselectivity aided by a chiral phosphine ligand of the Xantphos series. |
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ISSN: | 2052-4129 2052-4110 2052-4129 2052-4110 |
DOI: | 10.1039/D2QO01253G |