A copper-catalyzed enantioselective arylalkynylation of alkenes with diaryliodonium salt and a monosubstituted alkyne is reported. The three-component coupling reactions proceed under mild reaction conditions with a broad substrate scope, leading to synthetically valuable 1,2-diaryl-3-butynes. The key to the success of this chemistry is the employment of the chiral bisoxazoline-phenylaniline (BOPA) ligand. A novel reaction pathway involving the phenyl radical generation under thermal copper catalysis is proposed according to mechanistic studies.
CITATION STYLE
Lei, G., Zhang, H., Chen, B., Xu, M., & Zhang, G. (2020). Copper-catalyzed enantioselective arylalkynylation of alkenes. Chemical Science, 11(6), 1623–1628. https://doi.org/10.1039/c9sc04029c
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