A stereochemical surprise at the late stage of the synthesis of fully N-differentiated heparin oligosaccharides containing amino, acetamido, and N-sulfonate groups

Journal of Organic Chemistry

Volumn 69, Issue 12, 2004, Pages 4081-4093

  Lohman, Gregory J S ^a   Seeberger, Peter H ^a,b  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^b ETH ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; ETHERS; MIXTURES; POLYSACCHARIDES; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

GLUCOSAMINE; OLIGOSACCHRIDES;

OLIGOMERS;

ACETIC ACID; ACETIC ACID ESTER; ACETOACETIC ACID; DISACCHARIDE; GLYCOSAMINOGLYCAN; GLYCOSIDE; HEPARIN; HEPARIN DERIVATIVE; HEPARIN SACCHARIDE; IDURONIC ACID; NITROGEN; OLIGOSACCHARIDE; SULFONIC ACID DERIVATIVE; TETRASACCHARIDE; TETRASACCHARIDE TRICHLOROACETIMIDATE; UNCLASSIFIED DRUG;

ARTICLE; CARBOHYDRATE ANALYSIS; CHEMICAL BINDING; CHEMICAL STRUCTURE; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

CARBOHYDRATE CONFORMATION; HEPARIN; OLIGOSACCHARIDES;

EID: 2942536229     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035732z     Document Type: Article

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