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Dialkynyldiboranes(4) and the selectable reactivity of their C-H, C[triple bond, length as m-dash]C and B-B bonds.

作者信息

Schorr Fabian, Fantuzzi Felipe, Dewhurst Rian D, Braunschweig Holger

机构信息

Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, Würzburg 97074, Germany.

出版信息

Chem Commun (Camb). 2021 Mar 11;57(21):2645-2648. doi: 10.1039/d1cc00265a.

Abstract

The synthesis and reactivity of dialkynyldiboranes(4), a little-studied family of diboranes, are presented herein. Three dialkynyldiboranes(4) were prepared via two different salt metathesis pathways. The three reactive sites of these dialkynyldiboranes(4) are then selectively addressed by judicious application of reagents: addition of an amine N-oxide leads to oxygen insertion into the B-B bond, dicobaltoctacarbonyl binds to the alkynyl C[triple bond, length as m-dash]C bonds, while Sonogashira-Hagihara cross-coupling conditions lead to double C-C bond formation at the alkynyl C-H groups.

摘要

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