6533b852fe1ef96bd12ab5de

RESEARCH PRODUCT

Synthesis of sialyl-Tn antigen. Regioselective sialylation of a galactosamine threonine conjugate unblocked in the carbohydrate portion

Beate LiebeHorst Kunz

subject

Sialyl Tn antigenStereochemistryOrganic ChemistryRegioselectivityCarbohydrateBiochemistrycarbohydrates (lipids)chemistry.chemical_compoundBiochemistrychemistryAntigenGalactosamineDrug DiscoveryThreonineConjugate

description

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 .

https://doi.org/10.1016/s0040-4039(00)78495-4