Abstract
Synthetic study of the C'D'E' ring system of maitotoxin was examined via Suzuki-Miyaura coupling of an exo-iodoolefin and a furanylborane derivative, followed by Sharpless asymmetric dihydroxylation, Achmatowicz reaction, borylation/oxidation, and reductive etherification.
Original language | English |
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Pages (from-to) | 2313-2318 |
Number of pages | 6 |
Journal | Heterocycles |
Volume | 102 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2021 |
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Pharmacology
- Organic Chemistry