Model studies aimed at the synthesis of Fredericamycin A. A simple o-quinodimethane route to the spiro naphthalene portion
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (18) , 1983-1986
- https://doi.org/10.1016/s0040-4039(00)84427-5
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Access to the spiro hydrindandione ring system of Fredericamycin A through spiroalkylation and oxidation.Tetrahedron Letters, 1985
- Synthesis of 2,2-disubstituted 4,9-dihydroxy-1h-benz(f)indene-1,3(2h)diones. a model sequence for the synthesis of fredericamycinTetrahedron Letters, 1985
- Synthesis of the spirocyclic center of fredericamycin a by phenoxy-enoxy radical couplingTetrahedron Letters, 1985
- The “super-basic” butyllithium/potassium tert-butoxide mixture and other lickor-reagentsTetrahedron Letters, 1984
- Ring expansion and cleavage of succinoin derivatives. Geminal acylation, reductive succinoylation, and stereoselective spiro annelation methodsJournal of the American Chemical Society, 1984
- Syntheses of polycyclic ring systems based on the new generation of o-quinodimethanesJournal of the American Chemical Society, 1982
- Fredericamycin A, an antitumor antibiotic of a novel skeletal typeJournal of the American Chemical Society, 1982