Glycosylated vinyl ethers by the Julia-Lythgoe-Kocienski olefination: application to the synthesis of 2′,5′-dideoxydisaccharides and carbohydrated β-lactams

Tetrahedron Asymmetry

Volumn 20, Issue 14, 2009, Pages 1646-1660

  Sánchez, Iván Pérez ^a   Turos, Edward ^a  

^a Center for Molecular Diversity in Drug Design Discovery and Delivery   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2',5' DIDEOXYDISACCHARIDE DERIVATIVE; ALDEHYDE DERIVATIVE; BETA LACTAM DERIVATIVE; CARBOHYDRATE DERIVATIVE; GALACTOSE; GLUCOSE; ISOCYANIC ACID DERIVATIVE; RIBOSE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CHEMICAL REACTION; CYCLOADDITION; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; GLYCOSYLATION; JULIA LYTHGOE KOCIENSKI OLEFINATION; OLEFINATION; ONE POT SYNTHESIS; PRIORITY JOURNAL; ROOM TEMPERATURE; STAPHYLOCOCCUS AUREUS; STEREOCHEMISTRY;

EID: 68149083009     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.05.039     Document Type: Article

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