http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02264786-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_18a7d1606da2ec2ad08ae63822efb00e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-675
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6509
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 1989-04-05^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efdeb09ab931fd71e4108f94fce8457b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7a7d6811458152e3a60eb13ae7e44f4
publicationDate 1990-10-29^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02264786-A
titleOfInvention Heteroaryl alaphosphaline derivative
abstract NEW MATERIAL:A compound of the formula (R is heteroaryl). n EXAMPLE: 1-[(N-quinoxaloyl-L-alanyl)-amino]ethyl phosphonic acid. n USE: Anti-fungus agents. Little in side effects. n PREPARATION: Alaphosphaline and a heteroarylcarboxylic acid chloride (e.g. pyrazinecarboxylic acid chloride, quinoxaline carboxylic acid chloride) are made to react at low temperatures in an organic solvent in the presence of a base as dehydrochlorinating agent. n COPYRIGHT: (C)1990,JPO&Japio
priorityDate 1989-04-05^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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