SCOPUS 정보 검색 플랫폼

Carbohydrate Research

Volumn 403, Issue , 2015, Pages 69-89

In a glycosylation reaction how does a hydroxylic nucleophile find the activated anomeric carbon?

(1) Whitfield, Dennis M a

a NATIONAL RESEARCH COUNCIL CANADA (Canada)

Author keywords

Antiperiplanar lone pair hypotheses; Glycosylation; Nucleophile; Oxacarbenium ion; Solvation

Indexed keywords

CARBON; CHEMICAL BONDS; CHEMICAL COMPOUNDS; DENSITY FUNCTIONAL THEORY; ESTERIFICATION; GLYCOSYLATION; SOLVATION;

ANOMERIC CARBON; ANTIPERIPLANAR; BONDING INTERACTIONS; ELECTRON DEFICIENCY; GLYCOSYLATION REACTIONS; LONE PAIR; OXACARBENIUM IONS; POLAR ADDITIVES;

NUCLEOPHILES;

ACETONITRILE; ACETONITRILE DERIVATIVE; ACTIVATED ANOMERIC CARBON; ACTIVATED CARBON; ALPHA TRIFLATE; BETA METHANOL; CARBON; GLYCOSIDE; HYDROXIDE; HYDROXIDE ION; HYDROXYL GROUP; METHANOL; NUCLEOPHILE; OXYGEN; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

CARBOHYDRATE ANALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; DENSITY FUNCTIONAL THEORY; GLYCOSYLATION; HYDROGEN BOND; HYDROLYSIS; NUCLEOPHILICITY; PRIORITY JOURNAL; PROTON TRANSPORT; QUANTUM THEORY; REVIEW; STEREOCHEMISTRY; STEREOISOMERISM;

ACETONITRILES; CARBOHYDRATE CONFORMATION; CARBON; CHEMISTRY; GLYCOSIDES; GLYCOSYLATION; HYDROGEN BONDING; HYDROXIDES; METHANOL; MODELS, MOLECULAR; QUANTUM THEORY; STEREOISOMERISM;

EID: 85027921351 PISSN: 00086215 EISSN: 1873426X Source Type: Journal
DOI: 10.1016/j.carres.2014.05.021 Document Type: Review

Times cited : (18)

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