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filingDate 1982-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0ef58b90e73de175572afbaec5e8294
publicationDate 1984-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S59108762-A
titleOfInvention Synthetic intermediate for carbacycline compound and its preparation
abstract NEW MATERIAL:The compound of formula I [R 1 is H or OH-protecting group; R 2 is formyl or group of formula II (R 3 is substitutable alkyl, alkenyl, etc.); Ar is aryl; Y is S or Se; Z is O or carbonyl-protecting group]. n EXAMPLE: 2β-(2'-Methoxyvinyl)-3α-(2'-tetrahydropyranyloxy)-7, 7-ethylenedioxybicyclo[3,3,0]octane. n USE: A synthetic intermediate of carbacycline compound useful as a remedy for thrombosis, etc. n PROCESS: The objective compound of formula I can be prepared by reacting the compound of formula III with the ylide compound of formula IV (R 4 is aryl; R 5 is lower alkyl), and reacting the resultant compound of formula V with the compound of formula Ar-Y-X (e.g. benzene-sulfenyl chloride) in the presence of a base such as NaHCO 3 , Na 2 CO 3 , KHCO 3 , etc. n COPYRIGHT: (C)1984,JPO&Japio
priorityDate 1982-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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