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 |
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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