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filingDate 1992-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e003021452ff608d91fe5e7dcc7db403
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publicationDate 1993-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05246995-A
titleOfInvention Process for producing optically active cyclic amine
abstract (57) [Summary] [Objective] A synthetic intermediate of an optically active antibacterial compound useful as a drug can be easily obtained. [Configuration] Formula 1 (In the formula, X 1 and X 2 each independently represent a halogen atom or a hydrogen atom, Y represents an oxygen atom, a sulfur atom, methylene, or a hydrogen atom or a nitrogen atom which may have a substituent 1, R represents an alkyl group having 1 to 6 carbon atoms) is hydrogenated in the presence of an iridium-optically active phosphine complex and a halogen-containing salt to give a compound represented by the formula 2 Stereoisomers of compounds of formula (wherein X 1 , X 2 , Y and R are as defined above) are selectively prepared.
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