http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0437799-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-32
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filingDate 1990-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77f5c7ce6af0884f17a7222b3ad8a93d
publicationDate 1991-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0437799-A1
titleOfInvention The diastereoselective preparation of phosphinate esters
abstract An increase in the diastereoselectivity resulting from the reaction of a phosphinic acid ester of the formulan with the halo ester of the formulan is achieved by carrying out the reaction in the presence of 4-methylmorpholine, diazabicyclooctane, quinuclidine, 1-methylpyrolidine, or cinchonidine. After removal of the R 3 protecting group and fractional crystallization, the resulting desired diastereomeric pair can be resolved, and the desired isomer can be coupled to 4-substituted L-proline to give compounds possessing angiotensin converting enzyme inhibition activity. In particular, the process is useful in producing the antihypertensive agent fosinopril sodium in increased yields.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02088149-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02088149-A3
priorityDate 1990-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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