Abstract
Eponemycin, an antitumor and antiangiogenic epoxy ketone natural product, is previously shown to target proteasome for its activity. Although there have been many synthetic approaches developed, practical and efficient synthetic strategy for eponemycin has yet to be accomplished. Here, we report an efficient new route for the preparation of dihydroeponemycin, an active eponemycin derivative. This will aid the design of proteasome inhibitors with novel activity.
Original language | English |
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Pages (from-to) | 4829-4834 |
Number of pages | 6 |
Journal | European Journal of Organic Chemistry |
Issue number | 22 |
DOIs | |
State | Published - Nov 11 2005 |
Keywords
- Baylis-Hillman reaction
- Dihydroeponemycin
- Immunoproteasome
- Phosphonate
- Wittig-Horner reaction
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry