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Copper-catalyzed enantioselective desymmetrization of prochiral tetrasubstituted siladiols: Access toward optically active silicon-stereogenic silylmethanols

Qing Wang, Fei Ye, Jian Cao, Zheng Xu, Zhan‐Jiang Zheng, Li‐Wen Xu

2020Catalysis Communications19 citationsDOIOpen Access PDF

Abstract

A copper/pyridinebisoxazoline-catalyzed desymmetrization of prochiral 2-sila-1,3-propanediols with benzoyl chlorides has been described. The catalytic system allowed the construction of optically active silymethanol derivatives containing a quaternary siliconstereogenic center in good to high yields and moderate to good enantiomeric excesses.

Topics & Concepts

DesymmetrizationStereocenterEnantioselective synthesisOptically activeCatalysisChemistryCopperEnantiomerOrganic chemistryCombinatorial chemistryOrganoboron and organosilicon chemistryAsymmetric Synthesis and CatalysisSynthetic Organic Chemistry Methods
Copper-catalyzed enantioselective desymmetrization of prochiral tetrasubstituted siladiols: Access toward optically active silicon-stereogenic silylmethanols | Litcius