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Updated: May 16, 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
06:31

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

Ligand-Controlled Chemoselective and Enantioselective Cyclization of Enynes With Aroyl Chlorides

Zhen-Yu Wang1,2,3, Ling-Xia Zhang4, Yuqing Jiang5

  • 1Shanghai Frontiers Science Center for Drug Target Identification and Delivery, National Key Laboratory of Innovative Immunotherapy, and Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai, China.

Angewandte Chemie (International Ed. in English)
|May 14, 2026
PubMed

Keywords:
aroyl chloridescyclizationdecarbonylationenantioselectivityquaternary stereocenters

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