Convenient synthesis and biological activities of pyridine derivatives of 3,4-dihydropyrimidin-2(1H)-ones

Journal of Heterocyclic Chemistry

Volumn 48, Issue 3, 2011, Pages 572-576

  Zhu, Xiao Fei ^a   Shi, De Qing ^a  

^a CENTRAL CHINA NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLORODPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 ARYL 1,6 DIHYDROPYRIMIDIN 5 YL]CARBOXYLATE; 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 (4 NITROPHENYL) 1,6 DIHYDROPYRIMIDIN 5 YL]ETHANONE; 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 (4 TOLYL) 1,6 DIHYDROPYRIMIDIN 5 YL]ETHANONE; 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 (THIOPHEN 2 YL) 1,6 DIHYDROPYRIMIDIN 5 YL]ETHANONE; 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 PHENYL 1,6 DIHYDROPYRIMIDIN 5 YL]ETHANONE; 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 6 (4 METHOXYPHENYL) 4 METHYL 1,6 DIHYDROPYRIMIDIN 5 YL]ETHANONE; 1 [6 (4 CHLOROPHENYL) 1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 1,6 DIHYDROPYRIMIDIN 5 YL]ETHANONE; 2 CHLORO 5 (CHLOROMETHYL) PYRIDINE; ACETAMIPRID; CARBOXYLIC ACID DERIVATIVE; ETHYL 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 (4 TOLYL) 1,6 DIHYDROPYRIMIDIN 5 YL]CARBOXYLATE; ETHYL 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 4 METHYL 6 PHENYL 1,6 DIHYDROPYRIMIDIN 5 YL]CARBOXYLATE; ETHYL 1 [1 (6 CHLOROPYRIDIN 3 YL METHYL) 2 (6 CHLOROPYRIDIN 3 YL METHYLTHIO) 6 (4 METHOXYPHENYL) 4 METHYL 1,6 DIHYDROPYRIMIDIN 5 YL]CABOXYLATE; IMIDACLOPRID; NITENPYRAM; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BIOASSAY; CRYSTAL; DRUG STRUCTURE; DRUG SYNTHESIS; FUNGICIDAL ACTIVITY; INSECTICIDAL ACTIVITY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION;

EID: 79957490883     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.390     Document Type: Article

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