6533b852fe1ef96bd12ab5de
RESEARCH PRODUCT
Synthesis of sialyl-Tn antigen. Regioselective sialylation of a galactosamine threonine conjugate unblocked in the carbohydrate portion
Beate LiebeHorst Kunzsubject
Sialyl Tn antigenStereochemistryOrganic ChemistryRegioselectivityCarbohydrateBiochemistrycarbohydrates (lipids)chemistry.chemical_compoundBiochemistrychemistryAntigenGalactosamineDrug DiscoveryThreonineConjugatedescription
Abstract Regioselective and stereocontrolled formation of the sialyl-Tn antigen conjugate 6 was achieved by reacting the NeuNAc-2-xanthate 2 with the GalNAc threonine acceptor 5 bearing three hydroxy groups. Complete deprotection afforded the sialyl-Tn antigen structure 11 .
year | journal | country | edition | language |
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1994-11-01 | Tetrahedron Letters |