http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0323907-A2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-6561
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6561
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1989-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f41aed88907377ecd773ec0657ce63d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e34dfc9b54844c75d95df54022a5cd62
publicationDate 1989-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0323907-A2
titleOfInvention Preparation of 5,8,13,14-tetrahydrobenz(5,6)isoindolo (2,1-b)isoquinolin-8,13-dione derivatives
abstract A process is described for the preparation of compounds of formula (1)n [where OR is hydroxyl, protected hydroxyl or OP(O)(OCH₂Ph)(OR¹) (where Ph is phenyl and OR¹ is hydroxyl or protected hydroxyl)] and salts thereof, which comprises reacting a compound of formula (2)n with a compound of formula (3)n (where OR is as defined above and one of X¹ and X² is a leaving group and the other is a hydrogen atom) or a salt thereof, followed, if desired, by removal of the hydroxyl protecting group when present and/or by salt formation. n The compounds of formula (1) are either anticancer agents or intermediates useful in the synthesis of anticancer agents.
priorityDate 1988-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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