O-2 Substituted pyranosyl oxacarbenium ions are C-2-O-2 2-fold rotors with a strong syn preference

Carbohydrate Research

Volumn 342, Issue 18, 2007, Pages 2793-2800

  Ionescu, Andrei R ^a   Whitfield, Dennis M ^a   Zgierski, Marek Z ^a  

^a NATIONAL RESEARCH COUNCIL CANADA   (Canada)

Author keywords

Density functional theory; Glycosyl processing enzymes; Glycosylation; Natural bond order analysis; Quantum chemistry

Indexed keywords

GLYCOSYL PROCESSING ENZYMES; NATURAL BOND ORDER (NBO); OXACARBENIUM IONS; PYRANOSYL OXACARBENIUM IONS; STEREOELECTRONIC EFFECTS;

CARBON; DENSITY FUNCTIONAL THEORY; GLYCOSYLATION; QUANTUM CHEMISTRY; STABILITY;

CARBOHYDRATES;

GLYCOPYRANOSIDE; GLYCOSIDE; ION; O 2 TETRAHYDROPYRANOSYL OXACARBENIUM ION DERIVATIVE; PYRANOSYL OXACARBENIUM ION DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; GLYCOSYLATION; PRIORITY JOURNAL;

CARBOHYDRATE CONFORMATION; GLYCOSIDES; GLYCOSYLATION; IONS; ROTATION; STEREOISOMERISM;

EID: 36248959190     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2007.09.007     Document Type: Article

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