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
Hauptverfasser: Zhou, Xiao-Hua, Fang, Xiao-Jun, Ling, Fang-Ying, Xu, Zheng, Hong, Li-Quan, Ye, Fei, Xu, Li-Wen
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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.
ISSN:2052-4129
2052-4110
2052-4129
2052-4110
DOI:10.1039/D2QO01253G