The derivation of a chiral substituent code for secondary alcohols and its application to the prediction of enantioselectivity-Reference-Cited by-同舟云学术

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The derivation of a chiral substituent code for secondary alcohols and its application to the prediction of enantioselectivity

Published:2013-06 Issue: Volume:43 Page:11-20
ISSN:1093-3263
Container-title:Journal of Molecular Graphics and Modelling
language:en
Short-container-title:Journal of Molecular Graphics and Modelling

Author:

Suo Jing-Jie,Zhang Qing-You,Li Jing-Ya,Zhou Yan-Mei,Xu Lu

Publisher

Elsevier BV

Subject

Materials Chemistry,Computer Graphics and Computer-Aided Design,Physical and Theoretical Chemistry,Spectroscopy

Reference32 articles.

1. High-throughput methods for the development of new catalytic asymmetric reactions;Traverse;Drug Discovery Today,2002

2. Structure-based classification of chemical reactions without assignment of reaction centers;Zhang;Journal of Chemical Information and Modeling,2005

3. Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocampheylchloroborane, an exceptionally efficient chiral reducing agent;Brown;Journal of the American Chemical Society,1988

4. Asymmetric reduction with chiral organoboranes based on alpha-pinene;Brown;Accounts of Chemical Research,1992

5. Selective reductions. 52. Efficient asymmetric reduction of α-acetylenic α′-fluoroalkyl ketones with either B-chlorodiisopinocampheylborane or B-isopinocampheyl-9-borabicyclo[3.3.1]nonane in high enantiomeric purity. The influence of fluoro groups in such reductions

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3. Prediction on separation factor of chiral arylhydantoin compounds and recognition mechanism between chiral stationary phase and the enantiomers;Journal of Molecular Graphics and Modelling;2020-01

4. Quantitative Structure–Selectivity Relationships in Enantioselective Catalysis: Past, Present, and Future;Chemical Reviews;2019-12-30

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