The sulfonamidoglycosylation of benzylated glycals using a catalytic amount of triphenylphosphine hydrobromide proceeded in a highly stereoselective fashion to give the β anomers with good to high yields. This process was demonstrated with D-galactal and D-glucal. Two of the new N-2-(deoxyglycosyl)sulfonamides were tested as inhibitors of tumor cell growth in vitro and showed antiproliferative properties in the micromolar range.
Información general
Fecha de publicación:2003
Idioma del documento:Inglés
Revista:Organic Letters; vol. 5, no. 23
Institución de origen:Laboratorio de Estudio de Compuestos Orgánicos
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