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filingDate 2006-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3cd2fe5ab5281179ef1ad42b9d69f861
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publicationDate 2011-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2434847-C2
titleOfInvention Method for asymmetric alkynylation of alpha-iminoesters
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method of producing enantiomeric excess of asymmetrically alkynylated α-aminoesters of formula (III) in which R 1 and R 2 independently denote C 1-7 -alkyl, optionally substituted with phenyl or trimethylsilyl, or C 3-5 -cycloalkyl; Y denotes H or a nitrogen atom protecting group. The method involves reaction of α-iminoester of formula (I), in which R 1 and Y assume values given for formula III, with an alkyl containing a terminal triple bond, of formula (II), in which R 2 assumes values given for formula III, in the presence of a catalyst. The catalyst used contains a transition metal complex CuPF 6 ·4MeCN or CuOTf·0.5C 6 H 6 and a chiral ligand selected from , enantiomers thereof and mixture of enantiomers thereof. n EFFECT: method provides high output of asymmetrically alkynylated α-aminoesters of formula (III), which can be used in synthesis as optically active derivatives of amino acids which do not occur naturally. n 3 cl, 3 tbl, 4 ex
priorityDate 2005-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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