http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3772302-A

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filingDate 1971-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1973-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 1973-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3772302-A
titleOfInvention Processes and intermediates for quinine,quinidine,isomers and derivatives thereof
abstract THE PREPARATION OF QUININE, QUINIDINE, ISOMERS AND DERIVATIVES THEREOF FROM THE CORRESPONDINGLY SUBSTITUTED 4METHYLQUINOLINE AND 1-ACYL(OR 1-H)-3-VINYL(OR LOWER ALKYL)-4- PIPERIDINE ACETIC ACID ESTERS (OR ACETALDEHYDE) THROUGH ALTERNATIVE SERIES OF REACTION STEPS WHICH COMPRISE CONDENSATION, HALOGENATION, DECAYLATION, REDUCTION, CYCLIZATION AND HYDROXYLATION, IS DESCRIBED. ALSO DESCRIBED IS THE PREPARATION OF 1-ACYL(OR 1-H)-3-VINYL-4PIPERIDINEACETIC ACIDS AND ESTERS THEREOF AND 1-ACYL-3VINYL-4-PIPERIDINEACETALDEHYDE UTILIZING THE CORRESPONDING 7-ACYLDECAHYDRO-2H-PYRIDO(3,4-D)AZEPIN-2-ONE, PREPARED FROM -2ACYL-1,3,4,7,8,8A-HEXAHYDRO-6(2H)-ISOQUINOLONE. THE END PRODUCTS ARE USEFUL AS ANTIMALARIAL AND ANTIARRHYTHMIC AGENTS.
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP41522
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154085927
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13330322
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID5821
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450608741
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451165845
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID441074
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414024399
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID560818
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP81025
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419485969
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407182981
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP81423

Total number of triples: 312.