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Updated: Feb 22, 2026

Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators
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Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators

Published on: November 27, 2015

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Lewis Base-Catalyzed DYKAT of Racemic Chlorohydrosilanes With Grignard Reagents En Route to Si-Stereogenic

Yulang Tang1, Qi Zhou2, Shuya Li1

  • 1Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory For Plant-Sourced Drug, West China School of Pharmacy, Sichuan University, Chengdu, China.

Angewandte Chemie (International Ed. in English)
|February 21, 2026
PubMed

Keywords:
DYKATSi‐stereogenic organosilanesSi─C bond formationasymmetric catalysisenantioconvergent transformation

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