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Volumn 16, Issue 1, 2005, Pages 83-95

Synthesis of fully protected α-l-fucopyranosyl-(1→2)-β-d- galactopyranosides with a single free hydroxy group at position 2′, 3′ or 4′ using O-(2-naphthyl)methyl (NAP) ether as a temporary protecting group

(4) Szabó, Zoltán B a Borbás, Anikó a Bajza, István a Lipták, András a,b

a HAS UD Neuroscience Research Group (Hungary)

b UNIVERSITY OF DEBRECEN (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; BETA LEVO FLUCOPYRANOSIDE; DISACCHARIDE; ETHER DERIVATIVE; HYDROXYL GROUP; METHYL 3,4,6 TRI O BENZYL BETA DEXTRO GALACTOPYRANOSIDE; MONOSACCHARIDE; PHENYL 2,3 DI O BENZYL 4 O (2 NAPHTHYL)METHYL 1 THIO BETA LEVO FUCOPYRANOSIDE; PHENYL 2,4 DI O BENZYL 3 O (2 NAPHTHYL)METHYL 1 THIO BETA LEVO FUCOPYRANOSIDE; PHENYL 3,4 DI O BENZYL 2 O (2 NAPHTHYL)METHYL 1 THIO BETA LEVO FUCOPYRANOSIDE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL REACTION; GLYCOSYLATION; HYDROGENOLYSIS; METHYLATION; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS;

EID: 12344335423 PISSN: 09574166 EISSN: None Source Type: Journal
DOI: 10.1016/j.tetasy.2004.11.056 Document Type: Article

Times cited : (20)

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