Novel formal synthesis of stereospecifically C-6 deuterated d-glucose employing configurationally stable alkoxymethyllithiums

Tetrahedron

Volumn 66, Issue 3, 2010, Pages 591-598

  Kapeller, Dagmar C ^a   Hammerschmidt, Friedrich ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

Configurational stability; d Glucose; Deuterium labelling; Organolithiums; Stereospecificity

Indexed keywords

2,2,6,6 TETRAMETHYLPIPERIDINYL DERIVATIVE; 3 O BENZYL 1,2 O ISOPROPYLIDENE 6 O TETRAHYDROPYRANYL ALPHA DEXTRO GLUCOFURANOSE; 3 O BENZYL 1,2 O ISOPROPYLIDENE 6 O TETRAHYDROPYRANYL ALPHA LEVO IDOFURANOSE; ALDEHYDE; ALKOXYMETHYLLITHIUM; BENZALDEHYDE; BENZYL DERIVATIVE; DEUTERIUM; GLUCOSE; GLUCOSE DERIVATIVE; LITHIUM DERIVATIVE; PIPERIDINE DERIVATIVE; PYRAN DERIVATIVE; TIN DERIVATIVE; TRIBUTYLSTANNYLMETHYL 4 METHOXYBENZYL ETHER; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STABILITY; CHEMICAL STRUCTURE; CHIRALITY; CONFIGURATIONAL STABILITY; DEPROTECTION REACTION; ISOTOPE LABELING; MITSUNOBU REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOSPECIFICITY; SYNTHESIS; THERMOSTABILITY; WITTIG REARRANGEMENT;

EID: 71649090153     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.11.084     Document Type: Article

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