C-aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester

Journal of the American Chemical Society

Volumn 128, Issue 42, 2006, Pages 13696-13697

  Chen, Chi Li ^a   Sparks, Steven M ^a,b   Martin, Stephen F ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

^b GLAXOSMITHKLINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; GLYCOSIDE; UNCLASSIFIED DRUG; VINEOMYCINON B2 METHYL ESTER;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLOADDITION; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; HEATING; INTRAMOLECULAR BENZYME FURAN CYCLOADDITION; MITSUNOBU REACTION; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY;

ANTHRAQUINONES; ANTIBIOTICS, ANTINEOPLASTIC; BENZENE DERIVATIVES; CYCLIZATION; ESTERS; FURANS; GLYCOSIDES; METHYLATION; MODELS, CHEMICAL; STREPTOMYCES;

EID: 33750342526     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0652619     Document Type: Article

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