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Spirocyclic germanes via transannular insertion reactions of vinyl germylenes into Si–Si bonds†‡
Małgorzata Walewska,Judith Baumgartner,Christoph Marschner,Lena Albers,Thomas Müller
Dalton Transactions Pub Date : 03/23/2018 00:00:00 , DOI:10.1039/C8DT00315G
Abstract

The reactions of two cyclic germylene phosphane adducts with monosubstituted acetylenes caused the formation of spirocyclic germanes, which is postulated to occur by double acetylene insertion into germylene attached bonds. Further insertion of the formed cyclic divinylgermylene into transannular Si–Si or Si–Ge bonds provides the spirocyclic germanes. Thermal treatment of two germacyclopropenes, formed by the reaction of the two cyclic germylene phosphane adducts with tolane, also produced spirocyclogermanes. The structures of the latter require, however, a more complicated mechanistic proposal.

Graphical abstract: Spirocyclic germanes via transannular insertion reactions of vinyl germylenes into Si–Si bonds
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