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Updated: Jul 7, 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

Optimización de la enantioselectividad y actividad del catalizador utilizando ligandos achirales y meso

Anna M Costa1, Ciril Jimeno, Jason Gavenonis

  • 1P. Roy and Diane T. Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, USA.

Journal of the American Chemical Society
|June 13, 2002
PubMed
Resumen

Este estudio optimizó la catálisis asimétrica utilizando ligandos achirales, logrando altos excesos enantioméricos en la síntesis de 1-fenil-1-propanol. Este enfoque ofrece una nueva estrategia para desarrollar reacciones enantioselectivas eficientes.

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