Oxazaborolidine mediated asymmetric ketone reduction: prediction of enantiomeric excess based on catalyst structure-Reference-Cited by-同舟云学术

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Oxazaborolidine mediated asymmetric ketone reduction: prediction of enantiomeric excess based on catalyst structure

Published:2004-02 Issue:3 Volume:15 Page:519-523
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Hoogenraad Marcel,Klaus Guido M,Elders Niels,Hooijschuur Simone M,McKay Ben,Smith Alan A,Damen Eric W.P

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference12 articles.

1. A novel approach for screening discrete variations in organic synthesis

2. Understanding Stereoinductionin Catalysis via Computer: New Tools for Asymmetric Synthesis

3. Characterization of New Six-Membered Transition States of the Amino-Alcohol Promoted Addition of Dialkyl Zinc to Aldehydes

4. Molecular Descriptors in QSAR/QSPR;Karelson,2000

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