Abstract
The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). TADA product 28 is a key intermediate toward the total synthesis of 1.
Original language | English |
---|---|
Pages (from-to) | 351-364 |
Number of pages | 14 |
Journal | Heterocycles |
Volume | 77 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 1 2009 |
Keywords
- Marine Natural Product
- Nakiterpiosin
- Stille Coupling
- Synthetic Study
- Transannular Diels-Alder Reaction
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry