An efficient approach to enantiomerically pure fluorhydrins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. A Convenient Synthesis of 3-Fluorinated 2-Oxopropyl Sulphoxides from Fluorinated Lithium Acetates and 1-Lithioalkyl Sulphoxides
2. P. Bravo, S. De Munari, E. Piovosi, G. Resnati, Gazz. Chim. It., in press.
3. Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxides
4. Reduction of .beta.-keto sulfoxides: a highly efficient asymmetric synthesis of both enantiomers of allylic alcohols
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2. The influence of fluorine on the asymmetric reduction of fluoromethyl ketones;Journal of Fluorine Chemistry;2007-07
3. Regio- and stereoselective synthesis of vicinal fluorohydrins;Journal of Fluorine Chemistry;2004-06
4. Asymmetric Synthesis of Chiral Organofluorine Compounds: Use of Nonracemic Fluoroiodoacetic Acid as a Practical Electrophile and Its Application to the Synthesis of Monofluoro Hydroxyethylene Dipeptide Isosteres within a Novel Series of HIV Protease Inhibitors;Journal of the American Chemical Society;2001-07-07
5. Stereoselective Synthesis of Fluorinated Isoxazolidines and 2,3-Dihydroisoxazoles: A Cycloadditive Route to Enantiomerically Pure Amino Fluoro Alcohols;European Journal of Organic Chemistry;1999-07
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