Approach to polysubstituted 4-pyridones from N-Aryl acetoacetamides via a N to C 1,3-acyl migration mediated by sodium persulfate

Journal of Organic Chemistry

Volumn 77, Issue 17, 2012, Pages 7665-7670

  Zhang, Zhiguo ^a   Fang, Shiliang ^a   Liu, Qingfeng ^a   Zhang, Guisheng ^a  

^a HENAN NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

2-PYRIDONES; SELF-CONDENSATION; SODIUM PERSULFATE;

CONDENSATION; X RAY DIFFRACTION ANALYSIS;

SODIUM;

2 PYRIDONE DERIVATIVE; 2,6 DIMETHYL 4 OXO N,1 DI 4 TOLYL 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; 2,6 DIMETHYL 4 OXO N,1 DI M TOLYL 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; 2,6 DIMETHYL 4 OXO N,1 DI O TOLYL 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; 2,6 DIMETHYL 4 OXO N,1 DIPHENYL 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; 4 PYRIDONE DERIVATIVE; ACETAMIDE DERIVATIVE; ETHYL 4 [1 [4 (ETHOXYCARBONYL)PHENYL] 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDO]BENZOATE; N 1 BIS(2 CHLOROPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(2 METHOXYPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(2,4 DIMETHYLPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(3 CHLOROPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(4 CHLOROBENZYL) 2,4 DIMETHYL 6 OXO 1,6 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(4 CHLOROPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(4 ETHOXYPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(4 METHOXYBENZYL) 2,4 DIMETHYL 6 OXO 1,6 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(4 METHOXYPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 BIS(5 CHLORO 2 METHOXYPHENYL) 2,6 DIMETHYL 4 OXO 1,4 DIHYDROPYRIDINE 3 CARBOXAMIDE; N,1 DIBENZYL 2,4 DIMETHYL 6 OXO 1,6 DIHYDROPYRIDINE 3 CARBOXAMIDE; SODIUM SULFATE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; SYNTHESIS; X RAY DIFFRACTION;

ACETAMIDES; MOLECULAR STRUCTURE; PYRIDONES; SODIUM COMPOUNDS; SULFATES;

EID: 84866111125     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3010217     Document Type: Article

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