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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-18
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-25
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-42
filingDate 1969-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ec7b30f225a5326cedd5d31e29c27ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42937ffc612653f9caf473703dbff0cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5141e73c2f7436b9b82e641296b5c60e
publicationDate 1972-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-527793-A
titleOfInvention Process for the preparation of fluorenones, fluorenols and substituted fluorenes
abstract New cpds. of formula:- (where Z = O, H2 or H(OH); Y = O or S; X = the gp. -ANRR' or the gp. A = 2-8C alkylene; R and R' = H, lower alkyl, 3-6C cycloalkyl, 3-6C alkenyl or R and R' + N =pyrrolidine, piperidine, N-alkyl piperazine or morpholine; n = 0-2; m = 1 or 2; R2 = H, lower alkyl, 3-6C alkenyl) including their acid addn. salts have antiviral activity and may be administered, parenterally orally or topically in pharmaceutical compositions together with the usual carriers.
priorityDate 1968-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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