TOTAL SYNTHESIS OF MATURINONE THROUGH A REGIOSELECTIVE DIELS-ALDER REACTION OF 5-BROMINATED BENZOFURANDIONE

Authors
CHERKAOUI O NEBOIS P FILLION H
Citation
O. Cherkaoui et al., TOTAL SYNTHESIS OF MATURINONE THROUGH A REGIOSELECTIVE DIELS-ALDER REACTION OF 5-BROMINATED BENZOFURANDIONE, Chemical and Pharmaceutical Bulletin, 45(3), 1997, pp. 457-458
Citations number
25
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
Chemical and Pharmaceutical Bulletin → ACNP
ISSN journal
00092363
Volume
45
Issue
3
Year of publication
1997
Pages
457 - 458
Database
ISI
SICI code
0009-2363(1997)45:3<457:TSOMTA>2.0.ZU;2-C
Abstract
Maturinone was efficiently prepared by means of a regiocontrolled Diel s-Alder reaction between o-2-ethoxycarbonyl-3-methylbenzo[b]furan-4,7- dione 8 and penta-1,3-diene.