Convenient approaches to synthesis of furanoid sugar-aza-crown ethers from C-ribosyl azido aldehyde via a reductive amination/amidation

Yu Chi Hsieh; Jiun Ly Chir; Wei Zou; Hsiu Han Wu; An Tai Wu

doi:10.1016/j.carres.2009.03.008

Convenient approaches to synthesis of furanoid sugar-aza-crown ethers from C-ribosyl azido aldehyde via a reductive amination/amidation

Yu Chi Hsieh, Jiun Ly Chir, Wei Zou, Hsiu Han Wu, An Tai Wu

Department of Chemistry

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

14 Citations (Scopus)

Abstract

A short and highly efficient route to the α-anomer of a furanoid sugar-aza-crown ether was developed by a one-pot reductive amination of an α-anomer C-ribosyl azido aldehyde. In addition, the β-anomer furanoid sugar-aza-crown ether was synthesized from a linear disaccharide precursor via amidation and then followed by microwave-assisted amide reduction.

Original language	English
Pages (from-to)	1020-1023
Number of pages	4
Journal	Carbohydrate Research
Volume	344
Issue number	8
DOIs	https://doi.org/10.1016/j.carres.2009.03.008
Publication status	Published - 2009 May 26

All Science Journal Classification (ASJC) codes

Analytical Chemistry
Biochemistry
Organic Chemistry

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abstract = "A short and highly efficient route to the α-anomer of a furanoid sugar-aza-crown ether was developed by a one-pot reductive amination of an α-anomer C-ribosyl azido aldehyde. In addition, the β-anomer furanoid sugar-aza-crown ether was synthesized from a linear disaccharide precursor via amidation and then followed by microwave-assisted amide reduction.",

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AU - Chir, Jiun Ly

AU - Zou, Wei

AU - Wu, Hsiu Han

AU - Wu, An Tai

PY - 2009/5/26

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