http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1391082-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_db7324dd156e7b5744b5c160e3f02ccf
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-006
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D243-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D243-24
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D243-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D243-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D243-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-00
filingDate 1972-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1975-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1391082-A
titleOfInvention Optically active amino benzophenones
abstract 1391082 Amidobenzophenones CRC COMPAGNIA DI RICERCA CHIMICA SA 17 March 1972 [17 March 1971] 49556/74 Divided out of 1391081 Heading C2C S-Compounds of the general formula (R<SP>1</SP> = H, halogen, NO 2 : R<SP>2</SP> = H, C 1-4 alkyl; R<SP>3</SP> = C 1-4 alkyl, benzyl, substituted benzyl; A = protecting group) are prepared by acylating the corresponding 2-aminobenzophenone.
priorityDate 1971-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394834
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421025396
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID76080

Total number of triples: 19.