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 |
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Pages (from-to) | 1020-1023 |
Number of pages | 4 |
Journal | Carbohydrate Research |
Volume | 344 |
Issue number | 8 |
DOIs | |
Publication status | Published - 2009 May 26 |
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Biochemistry
- Organic Chemistry