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The exploitation of chirality at silicon in asymmetric catalysis is a challenging task. Silicon-stereogenic silanes were initially utilized to elucidate the stereochemical course of substitution at silicon. These mechanistic investigations are to be seen alongside a handful of synthetic transformations with covalently bound silicon as the stereoinducer. While in these substrate-controlled reactions the asymmetrically substituted silicon functions as a chiral auxiliary, reagent-controlled processes have remained elusive. This account summarizes the aimed design of silicon-stereogenic silanes and their introduction to stereoselective synthesis as chiral reagents.
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Martin Oestreich (Mon,) studied this question.
synapsesocial.com/papers/69dd4ed03f27c4971e99b3ec — DOI: https://doi.org/10.1055/s-2007-980385
Martin Oestreich
Technische Universität Berlin
Synlett
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