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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1804
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
filingDate 1997-08-04^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-12-15^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93874dd858a3fc7ba8ac42e902d14ba7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_049808631efc7ef0e5851528f9885f06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5bc52739bb5ba9f97a0d5a7ea14cd98
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4a3190e54d6e76d73d3033ef485b757
publicationDate 1998-12-15^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5849914-A
titleOfInvention Compounds formed by an asymmetric conjugate addition reaction
abstract This invention relates to a key intermediate in the synthesis of an endothelin antagonist and the synthesis of this key intermediate using an asymmetric conjugate addition reaction.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7425557-B2
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priorityDate 1996-08-09^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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