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Synthesis of a highly enantiomerically enriched silyllithium compound
Carsten Strohmann,Jan Hörnig,Dominik Auer
Chemical Communications Pub Date : 03/12/2002 00:00:00 , DOI:10.1039/B111687H
Abstract

The highly enantiomerically enriched silyllithium compound lithiomethylphenyl(1-piperidinylmethyl)silane (4) reacts stereospecifically with chlorosilanes, but over a period of several hours slow racemization in solution at room temperature occurs, which can be supressed by a transmetalation reaction with MgBr2(thf)4.

Graphical abstract: Synthesis of a highly enantiomerically enriched silyllithium compound
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