4.7 Article

A general method for asymmetric arylation and vinylation of silyl ketene acetals

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 1, Issue 4, Pages 365-367

Publisher

CHINESE CHEMICAL SOC
DOI: 10.1039/c4qo00027g

Keywords

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Funding

  1. Singapore National Research Foundation [NRF-RF2008-10]
  2. Nanyang Technological University

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A new biarylmonophosphine was developed for highly asymmetric arylation and vinylation of silyl enolates of acyclic esters with good generality. The new stereocenters alpha to the ester groups were formed in high enantiomeric excess. The method was applied to the asymmetric synthesis of Profen drugs on a gram scale.

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