A de novo synthesis of 2,6-dideoxy-C-Aryl glycosides based on ring closing metathesis and diastereoselective epoxide cleavage/anomerization reactions

Organic Letters

Volumn 2, Issue 6, 2000, Pages 791-794

  Schmidt, Bernd ^a  

^a TU DORTMUND UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; DEOXYSUGAR; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; GLYCOSIDE; TRIACYLGLYCEROL LIPASE;

ARTICLE; BURKHOLDERIA CEPACIA; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; ENZYMOLOGY; STEREOISOMERISM; SYNTHESIS;

ALCOHOLS; BURKHOLDERIA CEPACIA; DEOXY SUGARS; GLYCOSIDES; INDICATORS AND REAGENTS; LIPASE; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 0034704628     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005522y     Document Type: Article

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49. 3OD) δ 160.6, 135.1, 128.4, 114.6, 78.8, 78.4, 77.5, 73.8, 55.7, 42.7, 18.5.