Synthesis of N-glycyl-β-glycopyranosylamines, derivatives of main human secreted oligosaccharide core structures


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β-Glycopyranosylamines were synthesized by the reaction of ammonium carbamate with di-, tetra-, and hexasaccharides, corresponding to the human milk and urine oligosaccharide core structures, in aqueous methanolic solution in the presence of NH3. The N-acylation of these β-glycopyranosylamines with N-Boc-glycine N-hydroxysuccinimide ester followed by removal of the Boc group afforded N-glycyl-β-glycopyranosylamines of the corresponding oligosaccharides in yields of up to 60%.

作者简介

L. Likhosherstov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

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Email: likhosherstov@mail.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

O. Novikova

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: likhosherstov@mail.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

N. Kolotyrkina

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: likhosherstov@mail.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

V. Piskarev

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: likhosherstov@mail.ru
俄罗斯联邦, 28 ul. Vavilova, Moscow, 119991

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