Synthesis of N-protected azaoligosaccharides and their cyclic derivatives

Daisuke Sawada; Hideyo Takahashi; Moto Shiro; Shiro Ikegami

doi:10.1016/j.tetlet.2005.02.057

Synthesis of N-protected azaoligosaccharides and their cyclic derivatives

Daisuke Sawada, Hideyo Takahashi, Moto Shiro, Shiro Ikegami

Research output: Contribution to journal › Article › peer-review

12 Citations (Scopus)

Abstract

Azaoligosaccharides are prepared through the glycosylation of nojirimycin derivatives with catalytic amounts of TMSOTf. Also, the 1-6′, 1′-6-cyclic azadisaccharides are successfully synthesized, and their one-pot syntheses are demonstrated.

Original language	English
Pages (from-to)	2399-2403
Number of pages	5
Journal	Tetrahedron Letters
Volume	46
Issue number	14
DOIs	https://doi.org/10.1016/j.tetlet.2005.02.057
Publication status	Published - Apr 4 2005
Externally published	Yes

Keywords

Amino sugars
Azaoligosaccharide
Dimeric cycloazasugar

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2005.02.057

Cite this

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title = "Synthesis of N-protected azaoligosaccharides and their cyclic derivatives",

abstract = "Azaoligosaccharides are prepared through the glycosylation of nojirimycin derivatives with catalytic amounts of TMSOTf. Also, the 1-6′, 1′-6-cyclic azadisaccharides are successfully synthesized, and their one-pot syntheses are demonstrated.",

keywords = "Amino sugars, Azaoligosaccharide, Dimeric cycloazasugar",

author = "Daisuke Sawada and Hideyo Takahashi and Moto Shiro and Shiro Ikegami",

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doi = "10.1016/j.tetlet.2005.02.057",

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T1 - Synthesis of N-protected azaoligosaccharides and their cyclic derivatives

AU - Sawada, Daisuke

AU - Takahashi, Hideyo

AU - Shiro, Moto

AU - Ikegami, Shiro

PY - 2005/4/4

Y1 - 2005/4/4

N2 - Azaoligosaccharides are prepared through the glycosylation of nojirimycin derivatives with catalytic amounts of TMSOTf. Also, the 1-6′, 1′-6-cyclic azadisaccharides are successfully synthesized, and their one-pot syntheses are demonstrated.

AB - Azaoligosaccharides are prepared through the glycosylation of nojirimycin derivatives with catalytic amounts of TMSOTf. Also, the 1-6′, 1′-6-cyclic azadisaccharides are successfully synthesized, and their one-pot syntheses are demonstrated.

KW - Amino sugars

KW - Azaoligosaccharide

KW - Dimeric cycloazasugar

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DO - 10.1016/j.tetlet.2005.02.057

M3 - Article

AN - SCOPUS:17744396680

SN - 0040-4039

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EP - 2403

JO - Tetrahedron Letters

JF - Tetrahedron Letters

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ER -

Synthesis of N-protected azaoligosaccharides and their cyclic derivatives

Abstract

Keywords

ASJC Scopus subject areas

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