http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1707556-A4

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publicationDate 2007-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1707556-A4
titleOfInvention ENANTIOMER SELECTIVITY ENHANCED NUCLEOPHILIC ADDITION REACTION CONDUCTING METHOD FOR CONVERTING CARBONYL ENAMIDE, AND METHOD FOR SYNTHESIS OF OPTICALLY ACTIVE ALPHA-HYDROXY-GAMMA-KETO-ACID ESTER AND HYDROXYDICETONE ESTER
abstract A method of enantiometrically selective nucleophilic addition reaction to carbonyl, which enables asymmetric synthesis of optically active α-hydroxy-Ϝ-keto acid esters, optically active α-hydroxy-Ϝ-amino acid esters, hydroxydiketone compounds, etc. being useful as a raw material or synthetic intermediate for the production of pharmaceutical products, agricultural chemicals, perfumes, functional polymers, etc. In this method, the nucleophilic addition reaction of enamide compound accompanied by hydroxyl (-OH) formation to carbonyl is carried out in the presence of a chiral catalyst with copper or nickel.
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