Vilsmeier-haack reactions of 2-arylamino-3-acetyl-5,6-dihydro-4H-pyrans toward the synthesis of highly substituted pyridin-2(1H)-ones

Journal of Organic Chemistry

Volumn 72, Issue 22, 2007, Pages 8593-8596

  Xiang, Dexuan ^a   Yang, Yang ^a   Zhang, Rui ^b   Liang, Yongjiu ^b   Pan, Wei ^a   Huang, Jie ^a   Dong, Dewen ^a,b  

^a NORTHEAST NORMAL UNIVERSITY   (China)

^b CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ENAMINONES; HALOFORMYLATION; VILSMEIER-HAACK REACTIONS;

AROMATIC HYDROCARBONS; CYCLIZATION; NUCLEOPHILES; REACTION KINETICS;

SYNTHESIS (CHEMICAL);

3 ACETYL 5,6 DIHYDRO 4H PYRAN DERIVATIVE; FUNCTIONAL GROUP; HETEROCYCLIC COMPOUND; PYRAN DERIVATIVE; PYRIDIN 2(1H) ONE DERIVATIVE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; HALOFORMYLATION; INTRAMOLECULAR NUCLEOPHILIC CYCLIZATION; ONE POT SYNTHESIS; RING OPENING; SUBSTITUTION REACTION; VILSMEIER HAACK REACTION;

MOLECULAR STRUCTURE; PYRANS; PYRIDONES; STEREOISOMERISM;

EID: 35548931216     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7015482     Document Type: Article

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