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filingDate 1979-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c73ce4f71d53210ea866bad66bd750b0
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publicationDate 1980-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S55105638-A
titleOfInvention Aldol derivative and its preparation
abstract NEW MATERIAL:A 2-exo-formyl-3-endo-hydroxy-7-oxo-cis-bicyclo[3, 3, 0]octane shown by the formula I (C=W is carbonyl or carbonyl-protecting group) and its derivative. n EXAMPLE: 2-Exo-formyl-3-endo-hydroxy-7, 7-ethylenedioxy-cis-bicyclo[ 3, 3, 0 ]octane. n USE: A synthetic intermediate of a related compound of prostaglandin I 2 (PGI 2 ), that is, a synthetic intermediate of 6, 9 (0) methanoprostacyclin, which is chemically stabler than PGI 2 and has the relaxation action of the artery and the control action of agglutination of blood platelet. n PROCESS: An olefin derivative shown by the formula III is subjected to oxidative ring cleavage to give a dialdehyde derivative shown by the formula IV which is subjected to intramolecular aldol ring closure to prepare a compound shown by the formula I, from which the title 6, 9, (0) methanoprostacyclin shown by the formula V is obtained. n COPYRIGHT: (C)1980,JPO&Japio
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