Straightforward preparation of functionalized α-CF 2-galactosides through an oxygen to carbon acyl migration

Chemistry - A European Journal

Volumn 17, Issue 19, 2011, Pages 5238-5241

  Colombel, Sophie ^a   Sanselme, Morgane ^b   Leclerc, Eric ^a   Quirion, Jean Charles ^a   Pannecoucke, Xavier ^a  

^a INSA   (France)

^b UNIVERSITÉ DE ROUEN   (France)

Author keywords

fluorine; glycoconjugates; organolithium; radical reactions; reduction

Indexed keywords

ACYL MIGRATION; ANOMERIC POSITION; FUNCTIONALIZED; GLYCOCONJUGATES; INTRAMOLECULAR ADDITIONS; ORGANOLITHIUM; RADICAL REACTIONS; REDUCTION SEQUENCE;

FLUORINE; OXYGEN; REACTION KINETICS;

CARBOHYDRATES;

1 O (ALPHA GALACTOPYRANOSYL) 2 HEXACOSANOYLAMINO 1,3,4 OCTADECANETRIOL; ANTIFREEZE PROTEIN; CARBON; FLUORINATED HYDROCARBON; GALACTOSIDE; GALACTOSYLCERAMIDE; OXYGEN; TN ANTIGEN; TUMOR ANTIGEN;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ANTIFREEZE PROTEINS; ANTIGENS, TUMOR-ASSOCIATED, CARBOHYDRATE; CARBON; CATALYSIS; GALACTOSIDES; GALACTOSYLCERAMIDES; HYDROCARBONS, FLUORINATED; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; OXYGEN; STEREOISOMERISM;

EID: 79955046635     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201100183     Document Type: Article

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