N-Tetrachlorophthaloyl-protected trichloroacetimidate of glucosamine as glycosyl donor in oligosaccharide synthesis

Tetrahedron Letters

Volumn 36, Issue 30, 1995, Pages 5343-5346

  Castro Palomino, Julio C ^a   Schmidt, Richard R ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; GLUCOSAMINE DERIVATIVE;

ARTICLE; CARBOHYDRATE SYNTHESIS; DIASTEREOISOMER; GLYCOSYLATION; REDUCTION; STEREOCHEMISTRY;

STAPHYLOCOCCUS PHAGE 3A;

EID: 85047674110     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/00404-0399(50)1027F-     Document Type: Article

References (37)

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4. Glycosyl Imidates, 65. Efficient synthesis of the Lewis antigen X (Lex) family
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6. Synthesis of a GPI Anchor of Yeast(Saccharomyces cerevisiae)
7. Synthesis of Structural Elements of the Capsular Polysaccharide ofStreptococcus PneumoniaeType 14
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9. Synthesis ofN-Acetylneuraminic Acid Derivatives and Structural Analogues
10. Reductive Dephthalimidation: A Mild and Efficient Method for The N-Phthaumido Deprotection During Ougosaccharide Synthesis
11. Use of 4- Nitro-N-phthalimide as Protective Group of Primary Amines
12. The allyl ether as a protecting group in carbohydrate chemistry. Part V. Preparation of benzyl ethers of carbohydrates for use in oligosaccharide synthesis
13. Acidic Opening of 4,6-O-Orthoesters of Pyranosides