Volume 57, Issue 13 p. 3499-3503
Communication

Regioselective Cyclotrimerization of Terminal Alkynes Using a Digermyne

Tomohiro Sugahara

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011 Japan

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Dr. Jing‐Dong Guo

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011 Japan

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Prof. Dr. Takahiro Sasamori

Corresponding Author

Graduate School of Natural Sciences, Nagoya City University, Yamanohata 1, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, 467-8501 Japan

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Prof. Dr. Shigeru Nagase

Fukui Institute for Fundamental Chemistry, Kyoto University, Sakyo-ku, Kyoto, 606-8103 Japan

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Prof. Dr. Norihiro Tokitoh

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011 Japan

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First published: 07 February 2018
Citations: 18

Abstract

The catalytic activation of small neutral molecules followed by the formation of C−C bonds is a highly important method to increase the complexity and/or value of simple starting materials. Reported is an isolable digermyne, a compound with a Ge≡Ge bond, which acts as a precatalyst for the cyclotrimerization of terminal arylacetylenes to afford the corresponding 1,2,4‐triarylbenzenes with absolute regioselectivity. The results demonstrate that bespoke main‐group‐element compounds can catalytically activate and transform small neutral organic molecules and induce the formation of C−C bonds.

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