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Murai, Masahito Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University ORCID Kaken ID publons researchmap
Yamamoto, Masaki Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
A (μ-aryloxo)rhenium complex was isolated and confirmed as a key precatalyst for rhenium-catalyzed ortho-alkenylation (C-alkenylation) of unprotected phenols with alkynes. The reaction exclusively provided ortho-alkenylphenols; the formation of para or multiply alkenylated phenols and hydrophenoxylation (O-alkenylation) products was not observed. Several mechanistic experiments excluded a classical Friedel-Crafts-type mechanism, leading to the proposed phenolic hydroxyl group assisted electrophilic alkenylation as the most plausible reaction mechanism. For this purpose, the use of rhenium, a metal between the early and late transition metals in the periodic table, was key for the activation of both the soft carbon-carbon triple bond of the alkyne and the hard oxygen atom of the phenol, at the same time. ortho-Selective alkenylation with allenes also provided the corresponding adducts with a substitution pattern different from that obtained by the addition reaction with alkynes.
This is the peer reviewed version of the following article: [Masahito Murai et. al. Mechanistic Insights into Rhenium‐Catalyzed Regioselective C‐Alkenylation of Phenols with Internal Alkynes. Chemistry - A European Journal 25(66) 15189-15197 (2019), which has been published in final form at https://doi.org/10.1002/chem.201903910. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Chemistry - A European Journal
|Web of Science KeyUT|
Murai M, Yamamoto M, Takai K. Mechanistic Insights into Rhenium-Catalyzed Regioselective C-Alkenylation of Phenols with Internal Alkynes. Chemistry. 2019;25(66):15189‐15197. doi:10.1002/chem.201903910
Japan Society for the Promotion of Science