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 | |
| Publication status | Published - 2009 May 26 |
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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 journal › Article
TY - JOUR
T1 - Convenient approaches to synthesis of furanoid sugar-aza-crown ethers from C-ribosyl azido aldehyde via a reductive amination/amidation
AU - Hsieh, Yu Chi
AU - Chir, Jiun Ly
AU - Zou, Wei
AU - Wu, Hsiu Han
AU - Wu, An Tai
PY - 2009/5/26
Y1 - 2009/5/26
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=65149097159&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=65149097159&partnerID=8YFLogxK
U2 - 10.1016/j.carres.2009.03.008
DO - 10.1016/j.carres.2009.03.008
M3 - Article
C2 - 19362710
AN - SCOPUS:65149097159
VL - 344
SP - 1020
EP - 1023
JO - Carbohydrate Research
JF - Carbohydrate Research
SN - 0008-6215
IS - 8
ER -