Literature DB >> 16216041

Chirality transfer from silicon to carbon.

Martin Oestreich1.   

Abstract

The exploitation of the asymmetry at silicon in stereoselective synthesis is an exceptionally challenging task. Initially, silicon-stereogenic silanes have been utilized to elucidate the stereochemical course of substitution reactions at silicon. Apart from these mechanistic investigations, only a handful of synthetic applications with an asymmetrically substituted silicon as the stereochemical controller have been reported to date. In these transformations the chiral silicon functions as a chiral auxiliary. Conversely, a direct transfer of chirality from silicon to carbon during bond formation and cleavage at silicon has remained open until its recent realization in both inter- and intramolecular reactions. In this Concept, the pivotal considerations in relation to the nature of suitable silanes as well as mechanistic prerequisites for an efficient chirality transfer will be discussed.

Entities:  

Year:  2005        PMID: 16216041     DOI: 10.1002/chem.200500782

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Enantioselective Si-H Insertion Reactions of Diarylcarbenes for the Synthesis of Silicon-Stereogenic Silanes.

Authors:  Jake R Jagannathan; James C Fettinger; Jared T Shaw; Annaliese K Franz
Journal:  J Am Chem Soc       Date:  2020-06-24       Impact factor: 15.419

2.  Conformational rigidity of silicon-stereogenic silanes in asymmetric catalysis: A comparative study.

Authors:  Sebastian Rendler; Martin Oestreich
Journal:  Beilstein J Org Chem       Date:  2007-02-08       Impact factor: 2.883

3.  Chiral Control in Pentacoordinate Systems: The Case of Organosilicates.

Authors:  Leon J P van der Boon; Laurens van Gelderen; Tim R de Groot; Martin Lutz; J Chris Slootweg; Andreas W Ehlers; Koop Lammertsma
Journal:  Inorg Chem       Date:  2018-10-02       Impact factor: 5.165

  3 in total

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