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

Research output: Contribution to journalArticle

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 languageEnglish
Pages (from-to)1020-1023
Number of pages4
JournalCarbohydrate Research
Volume344
Issue number8
DOIs
Publication statusPublished - 2009 May 26

Fingerprint

Crown Ethers
Amination
Aldehydes
Sugars
Disaccharides
Microwaves
Amides

All Science Journal Classification (ASJC) codes

  • Analytical Chemistry
  • Biochemistry
  • Organic Chemistry

Cite this

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Convenient approaches to synthesis of furanoid sugar-aza-crown ethers from C-ribosyl azido aldehyde via a reductive amination/amidation. / Hsieh, Yu Chi; Chir, Jiun Ly; Zou, Wei; Wu, Hsiu Han; Wu, An Tai.

In: Carbohydrate Research, Vol. 344, No. 8, 26.05.2009, p. 1020-1023.

Research output: Contribution to journalArticle

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AU - Wu, An Tai

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