An Efficient Synthesis of 4-Halo-5-hydroxyfuran-2(5H)-ones via the Sequential Halolactonization and γ-Hydroxylation of 4-Aryl-2, 3-alkadienoic Acids

Journal of Organic Chemistry

Volumn 69, Issue 4, 2004, Pages 1429-1431

  Ma, Shengming ^a   Wu, Bin ^a   Shi, Zhangjie ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYLATION; ORGANIC ACIDS; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

HALOLACTONIZATION;

AROMATIC COMPOUNDS;

3 METHYL 4 IODO 5 PHENYL 5 HYDROXYL 2(5H) FURANONE; 5 HYDROXYFURAN 2(5H) ONE DERIVATIVE; ALKADIENE; ALKANOIC ACID; BROMINE DERIVATIVE; CHLORINE DERIVATIVE; FURANONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROXYLATION; REACTION ANALYSIS; X RAY DIFFRACTION;

EID: 1242307297     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0355698     Document Type: Article

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