Abstract
We report the first example of highly enantioselective organocatalytic synthesis of 3-difluoroalkyl substituted 3-hydroxyoxindoles. The total synthesis of the difluoro analogue of convolutamydine E was achieved by this method.
| Original language | English |
|---|---|
| Pages (from-to) | 1919-1921 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 48 |
| Issue number | 13 |
| DOIs | |
| State | Published - 16 Jan 2012 |
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