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

13 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

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All Science Journal Classification (ASJC) codes

Analytical Chemistry
Biochemistry
Organic Chemistry

Cite this

Hsieh, Y. C., Chir, J. L., Zou, W., Wu, H. H., & Wu, A. T. (2009). Convenient approaches to synthesis of furanoid sugar-aza-crown ethers from C-ribosyl azido aldehyde via a reductive amination/amidation. Carbohydrate Research, 344(8), 1020-1023. https://doi.org/10.1016/j.carres.2009.03.008

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Access to Document

10.1016/j.carres.2009.03.008