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Royal Society of Chemistry, Catalysis Science & Technology, 3(6), p. 863-868, 2016

DOI: 10.1039/c5cy01139f

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Hydrophenylation of internal alkynes with boronic acids catalysed by a Ni-Zn hydroxy double salt-intercalated anionic rhodium(III) complex

This paper is available in a repository.
This paper is available in a repository.

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Abstract

[Rh(OH)6]3− intercalated Ni–Zn mixed basic salt (Rh/NiZn) acts as an efficient catalyst for the hydrophenylation of internal alkynes with arylboronic acids under mild conditions. The turnover number per Rh site approached 740 in the reaction between 4-octyne and phenylboronic acid. The catalytic monomeric Rh(III) complex is stabilised within the NiZn interlayers, attributable to a strong electrostatic interaction, promoting its re-use.