Stereocontrolled syntheses of O-glycans of core class 2 with a linear tetrameric lactosamine chain and with three lactosamine branches

DOI: 10.1016/S0008-6215(96)90116-0

Source and publish data:

Carbohydrate Research p. 25 - 39 (1996)

Update date:2022-08-03

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Authors:

Wang, Zhi-Guang

Zhang, Xu-Fang

Ito, Yukishige

Nakahara, Yoshiaki

Ogawa, Tomoya

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Article abstract of DOI:10.1016/S0008-6215(96)90116-0

Synthetic routes to O-glycans of core class 2 with a linearly extended tetralactosamine moiety and with three lactosamine branches are discussed. By a glycosyl fluoride-method, the mono- and the di-lactosaminyl units were attached to the core disaccharide (Galβ1→3GalN₃) derivatives in high stereoselectivity.

Full text of DOI:10.1016/S0008-6215(96)90116-0

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