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Synthetic studies on maitotoxin. 1. Stereoselective synthesis of the C'D'E'F'-ring system having a side chain.
- Source :
-
Organic letters [Org Lett] 2008 May 01; Vol. 10 (9), pp. 1675-8. Date of Electronic Publication: 2008 Apr 08. - Publication Year :
- 2008
-
Abstract
- The stereoselective synthesis of the maitotoxin C'D'E'F'-ring system having a side chain has been accomplished through a convergent strategy. The key reactions include Horner-Wadsworth-Emmons coupling of the C'D'E'-ring and the side chain and subsequent construction of the F'-ring by silane reduction of dihydropyran.
- Subjects :
- Animals
Dinoflagellida chemistry
Ethers, Cyclic chemistry
Marine Toxins chemistry
Molecular Structure
Oxocins chemistry
Polycyclic Compounds chemistry
Stereoisomerism
Ethers, Cyclic chemical synthesis
Marine Toxins chemical synthesis
Oxocins chemical synthesis
Polycyclic Compounds chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1523-7060
- Volume :
- 10
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Organic letters
- Publication Type :
- Academic Journal
- Accession number :
- 18393510
- Full Text :
- https://doi.org/10.1021/ol800267x