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Regioselective Cyclotrimerization of Terminal Alkynes Using a Digermyne.
Sugahara, Tomohiro; Guo, Jing-Dong; Sasamori, Takahiro; Nagase, Shigeru; Tokitoh, Norihiro.
Afiliação
  • Sugahara T; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.
  • Guo JD; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.
  • Sasamori T; Graduate School of Natural Sciences, Nagoya City University, Yamanohata 1, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, 467-8501, Japan.
  • Nagase S; Fukui Institute for Fundamental Chemistry, Kyoto University, Sakyo-ku, Kyoto, 606-8103, Japan.
  • Tokitoh N; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.
Angew Chem Int Ed Engl ; 57(13): 3499-3503, 2018 03 19.
Article em En | MEDLINE | ID: mdl-29411488
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article