Pincer cobalt complex-catalyzed: Z -selective hydrosilylation of terminal alkynes

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Abstract

A phosphine-iminopyridine (PCNN) cobalt-catalyzed Z-selective hydrosilylation of terminal alkynes with Ph2SiH2 has been developed for the synthesis of (Z)-β-vinylsilanes with high regio- and stereoselectivity and wide functional group tolerance. Furthermore, the Co-catalyzed hydrosilylations of unsymmetrical arylalkyl disubstituted internal alkynes afford syn-addition products with unique regioselectivity: the silyl group is added to the alkyl-substituted carbon, instead of the aryl-substituted carbon. The (Z)-β-vinylsilane products are further applied to Pd-catalyzed Hiyama-Denmark cross-couplings for stereoselective synthesis of (Z)-disubstituted alkenes.

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Du, X., Hou, W., Zhang, Y., & Huang, Z. (2017). Pincer cobalt complex-catalyzed: Z -selective hydrosilylation of terminal alkynes. Organic Chemistry Frontiers, 4(8), 1517–1521. https://doi.org/10.1039/c7qo00250e

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