Abstract
Radicamine B 2, the enantiomer of natural radicamine B 5, was synthesized via a chiral nitrone derived from D-xylose in 10 steps with an overall yield of 15%. © 2007 Bentham Science Publishers Ltd.
Original language | English |
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Pages (from-to) | 556-558 |
Number of pages | 3 |
Journal | Letters in Organic Chemistry |
Volume | 4 |
Issue number | 8 |
DOIs | |
Publication status | Published - Dec 2007 |
Keywords
- D-xylose
- Enantiospecific synthesis
- Iminosugars
- Nitrone
- Radicamine B