http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6372672-A

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Predicate Object
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C401-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1986-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c78d50133246ed8b24f359ce49c9f0c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4637953de4fc8fd2a509946b9fc404c
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publicationDate 1988-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6372672-A
titleOfInvention 2-fluoro-4-hydroxy-2-cycropentenones and production thereof
abstract NEW MATERIAL:A compound expressed by formula I (R 1 is 1W10C alkyl; R 2 is alkyl or alkenyl; R 3 is H, tri 1W7C hydrocarbon silyl or group capable of forming a acetal bond with O of group; A and B are respectively H and OH or one bonding hand linked with A and B). n EXAMPLE: 2-Fluoro-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-octyl-4-trimethylsilyl oxy-2-cyclopentenone. n USE: Anticancer agent, showing strong action for inhibiting a cancer cell growth to especially leukemia bacterium in low concentration. n PREPARATION: 2-Fluoro-4-hydroxy-2-cyclopentenones expressed by formula II (R 30 is tri 1W7C hydrocarbon silyl or group capable of forming an acetal bond with O of OH) are subjected to aldol condensation reaction with aldehydes expressed by the formula OHC-C-R 10 (R 10 is 1W10C alkyl) and as necessary, followed by deprotection, hydrolysis and salt-forming reaction to provide a compound expressed by formula I. n COPYRIGHT: (C)1988,JPO&Japio
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priorityDate 1986-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 28.