Strategies and intermediates for fredericamycin a synthesis: A 3-substituted 9-alkoxy cyclopenta(g)isoquinoline-1,8(2H)-dione
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (33) , 3835-3838
- https://doi.org/10.1016/s0040-4039(00)83892-7
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A mercury-mediated acyl migration in a pinacol-type rearrangement. Model studies toward the synthesis of fredericamycin AThe Journal of Organic Chemistry, 1986
- Model studies aimed at the synthesis of Fredericamycin A. A simple o-quinodimethane route to the spiro naphthalene portionTetrahedron Letters, 1986
- Synthesis of spikdcyclic diketones related to fbedericamycim ATetrahedron Letters, 1986
- SYNTHESIS OF PHENOLS BY POLYKETIDE CONDENSATION AND AN EFFICIENT SYNTHESIS OF 3,5-DIOXOALKANOATES FROM AMIDESChemistry Letters, 1985
- Synthesis of methyl 3,5,9,11,13-pentaoxotetradecanoate, a "skipped" heptaketide, via ozonolysis of a hydroaromatic systemThe Journal of Organic Chemistry, 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
- Fredericamycin A, an antitumor antibiotic of a novel skeletal typeJournal of the American Chemical Society, 1982
- Synthesis of polyketide-type aromatic natural products by biogenetically modeled routesTetrahedron, 1977
- Aldol Type Condensations of β-Keto Ester DianionsCanadian Journal of Chemistry, 1974