| Autor: |
Gemma S; Dipartimento Farmaco Chimico Tecnologico (DFCT), University of Siena, via Aldo Moro 2, 53100 Siena, Italy., Gabellieri E, Sanna Coccone S, Martí F, Taglialatela-Scafati O, Novellino E, Campiani G, Butini S |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of organic chemistry [J Org Chem] 2010 Apr 02; Vol. 75 (7), pp. 2333-40. |
| DOI: |
10.1021/jo1001559 |
| Abstrakt: |
The first synthesis of the marine endoperoxide 9,10-dihydroplakortin, of its C10-desethyl analogue, and of their corresponding C6 epimers is described. Stereogenic centers at C4 and at the lateral chain have been stereoselectively synthesized through Evans' chiral auxiliary chemistry. Moreover, the reported synthesis features a one-pot three-step hydroperoxysilylation/cyclization reaction for the construction of the endoperoxide ring system. Homologation of the aldehyde resulting from diol cleavage through a Wittig-based strategy gave access to the ester-containing lateral chain at C3. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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