Toward the total synthesis of vineomycin B2: application of an efficient glycosylation methodology using 2,3-unsaturated sugars

Tetrahedron Letters

Volumn 48, Issue 39, 2007, Pages 6982-6986

  Sasaki, Kaname ^a   Matsumura, Shuichi ^a   Toshima, Kazunobu ^a  

^a KEIO UNIVERSITY   (Japan)

Author keywords

2,3 Unsaturated sugar; Chemoselectivity; Glycosylation; Ionic liquid; Vineomycin B2

Indexed keywords

2,3 GLYCOSYL ACETATE; ANTIBIOTIC AGENT; BETA OXO TERT ALCOHOL; DISACCHARIDE; RHODINOSE; SUGAR; UNCLASSIFIED DRUG; VINEOMYCIN B2;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; GLYCOSYLATION; HYDROGENATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 34548284976     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.07.145     Document Type: Article

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