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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B55-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C13-28
filingDate 1989-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e882a9aab5c64707e4ddef243d0c4b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed6a4f1b59e75809df1acadcbd3b4342
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_061457394d4131e774d2988eb71db65c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d7ea72baf6ad84f541632cc4fe35445
publicationDate 1991-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1680685-A1
titleOfInvention Method for splitting of racemic (1sr, 2 rs, 5r, 6rs)-bicyclo(3
abstract This invention relates to fine organic synthesis, in particular to the resolution of racemic (1SR, 2RS, 5SR, 6RS) -6H4rooio (3.3.0) oKTaH diol form I BUT gas-1 to obtain (IS, 2R, 5S, 6R) - 2,6-flH-acetoxy-bicyclo (3.3.0) octane of the formula II n3c- (o) s-oh II no-c (o) -cn3 and (1R, 2S, 5R, 63) -dicyclo (3.3.0) -Octane-2-diol f-ly III, non III n it can be used for the synthesis of optically active prostaglandins and their derivatives. In order to increase the yield and increase the enantiomeric excess of separable optical antipodes (1SR, 2RS, 5SR, 6RS) -6n-cyclo (3.3.0) octane-2, 6-diol is treated with 2,2,2-trichloroethyl acetate at 20 -40 ° C in the presence of pyridine or triethanolamine in anhydrous tetrahydrofuran. As an enzyme, lipases of animal origin are used, preferably crude lipase of porcine pancrease as a preparation. 1 hp f-ly. CO with Os 00 O o 00 SP
priorityDate 1989-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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