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filingDate 1990-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccc8e7532bf12d5f716ccdc12c6562e9
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publicationDate 1994-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H069633-A
titleOfInvention Enantioselective preparation method of (ω-1) -hydroxyalkylxanthine
abstract (57) [Summary] (Correction) [Constitution] The following formula I [In the formula, R 1 and R 2 R 3 are the same or different, and the substituents CH 3 —CO— (CH 2 ) m — and (C 1 -C 6) - is selected from the group consisting of alkyl, one of the group of substituents is CH 3 -CO- (CH 2) m , (C 1 -C 6 ) -alkyl is a straight chain or branched chain] compound of Rhodotorulabra DSM 54 S- (ω-1) consisting of incubating with 36 -A method for the enantioselective preparation of hydroxyalkylxanthines. [Effect] It has an effect of increasing cerebral blood flow.
priorityDate 1989-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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