http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2672050-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_682f5a24344011e5caf4eb35e036355b
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C243-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D271-107
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C243-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C241-04
filingDate 1991-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9495e3a982259fc00d6e7a133e3a8761
publicationDate 1992-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2672050-A1
titleOfInvention DIARYL-2,5-OXADIAZOLES 1,3,4-HYDROXYESTER, HYDROXYACIDE AND ACETOXYACIDE, PROCESS FOR THEIR SYNTHESIS.
abstract The invention relates to 2,5-diaryl oxadiazoles-1,3,4 with hydroxy ester, hydroxy acid and acetoxyacid endings of the formula: (CF DRAWING IN BOPI) in which R1 represents a hydroxyl or acetyl radical and R2 represents a carboxyl radical and where R1 and R2 preferably simultaneously occupy the 3 and 3 'or 4 and 4' positions. The hydroxyesters are prepared by cyclization of the corresponding diaromatic dihydrazide and the hydroxy acids are obtained by saponification of the preceding hydroxyesters.
priorityDate 1991-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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