Abstract
Synthetic entry to the ABCD ring fragment of gymnocin-A, a cytotoxic marine polyether, has been achieved based on the B-alkyl Suzuki-Miyaura coupling-based strategy and radical cyclization for the construction of the tetrahydrofuran ring A.
Original language | English |
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Pages (from-to) | 4351-4354 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 44 |
Issue number | 23 |
DOIs | |
Publication status | Published - 2003 Jun 2 |
Keywords
- B-alkyl Suzuki-Miyaura coupling
- Gymnocin-A
- Polycyclic ethers
- Radical cyclization
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry