http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02212474-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-90
filingDate 1989-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8c173b0244245a26f23ec4d1cf13bc8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fa60d88d2ba55246568e9dbbf7a4d6a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7980bac3cc1c51f46c2de219993286b6
publicationDate 1990-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02212474-A
titleOfInvention Production of optically active 1,4-dihydropyridine derivative
abstract PURPOSE: To obtain the title compound in high yield by reaction of a benzylidene-acetoacetic ester derivative with an optically active 2-aminocrotonic acid derivative in the presence of lithium amide followed by hydrolysis and reaction with an ammonium salt. n CONSTITUTION: A benzylidene-acetoacetic ester derivative of formula I (X, Y, Z are H, halogen, nitro where X, Y, Z do not represent H at a time: R 1 is lower alkyl) and an optically active 3-aminocrotonic ester derivative of formula II (R 2 is formula III: R 5 is lower alkyl, lower alkyloxy; R 6 is phenyl; n is 0, 1; R 3 , R 4 are lower alkyl; * is chiral center) are allowed to react in the presence of lithium amide, preferably lithium diisopropylamide at -80 to -70°C in an inert solvent. Then, the product is hydrolyzed, and allowed to react with an ammonium salt of formula IV (L is monovalent anion) to give the compound of formula V. n COPYRIGHT: (C)1990,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112679416-A
priorityDate 1989-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 26.