Abstract
Matrix presented An efficient and highly convergent synthesis of the FGHIJKLMN ring fragment of gymnocin A, a cyctotoxic polycyclic ether isolated from the notorious red-tide forming dinoflagellate Gymnodinium mikimotoi, has been achieved. The present synthesis relied on extensive use of the B-alkyl Suzuki-Miyaura coupling reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 1747-1750 |
| Number of pages | 4 |
| Journal | Organic letters |
| Volume | 4 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 2002 May 16 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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Sasaki, M., Tsukano, C., & Tachibana, K. (2002). Studies toward the total synthesis of gymnocin A, a cytotoxic polyether: A highly convergent entry to the F-N ring fragment. Organic letters, 4(10), 1747-1750. https://doi.org/10.1021/ol025814u