Synthesis of 1,4-dihydropyridine derivatives under solvent-free and grinding conditions

Synthetic Communications

Volumn 41, Issue 14, 2011, Pages 2152-2160

  Zonouz, Adeleh Moshtaghi ^a   Moghani, Davoud ^a  

^a AZARBAIJAN SHAHID MADANI UNIVERSITY   (Iran)

Author keywords

1,4 dihydropyridines; Grinding; Hantzsch reaction; Multicomponent reaction; Solvent free

Indexed keywords

1,4 DIHYDROPYRIDINE DERIVATIVE; ACETOACETIC ACID; AMMONIUM ACETATE; ETHYL 6 AMINO 5 CYANO 2 METHYL 4 (2 FURYL) 1,4 DIHYDROPYRIDINE 3 CARBOXYLATE; ETHYL 6 AMINO 5 CYANO 2 METHYL 4 (2 METHOXYPHENYL) 1,4 DIHYDROPYRIDINE 3 CARBOXYLATE; ETHYL 6 AMINO 5 CYANO 2 METHYL 4 (2 NITROPHENYL) 1,4 DIHYDROPYRIDINE 3 CARBOXYLATE; ETHYL 6 AMINO 5 CYANO 2 METHYL 4 (3 METHYLPHENYL) 1,4 DIHYDROPYRIDINE 3 CARBOXYLATE; ETHYL 6 AMINO 5 CYANO 2 METHYL 4 (3 NITROPHENYL) 1,4 DIHYDROPYRIDINE 3 CARBOXYLATE; ETHYL 6 AMINO 5 CYANO 2 METHYL 4 (4 NITROPHENYL) 1,4 DIHYDROPYRIDINE 3 CARBOXYLATE; MALONONITRILE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; DRUG PURIFICATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENERGY YIELD; GRINDING; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME;

EID: 79957632750     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397911.2010.499488     Document Type: Article

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