A stereoselective approach to the angucyclinone antibiotics: A total synthesis of the C-1 epimer of (±)-rubiginone B1
- 19 February 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (8) , 1373-1376
- https://doi.org/10.1016/s0040-4039(00)91799-4
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Synthetic studies of the angucycline antibiotics. Reaction of a quinone methide produced from a benz[a]anthracene with molecular oxygenThe Journal of Organic Chemistry, 1992
- Angucycline group antibioticsNatural Product Reports, 1992
- The synthesis of angularly fused aromatic ring systems. The synthesis of 3-deoxyrabelomycinTetrahedron Letters, 1991
- Studies on quinones. Part 21. Regioselective synthesis of tetracyclic quinones related to rabelomycinJournal of the Chemical Society, Perkin Transactions 1, 1991
- Chemical and biological properties of rubiginone, a complex of new antibiotics with vincristine-cytotoxicity potentiating activity.The Journal of Antibiotics, 1990
- A new route for the efficient synthesis of (±)ochromycinone, a naturally occurring benz[a] anthraquinone.Tetrahedron Letters, 1987
- Directed ortho metalation reactions. Synthesis of the naturally-occurring benz[a]anthraquinones X-14881 C and ochromycinoneTetrahedron Letters, 1985
- An approach to the synthesis of mevinolin based on intramolecular Diels-Alder cycloadditionThe Journal of Organic Chemistry, 1985
- A new dihydrobenz[a]anthraquinone antitumor antibiotic (PD 116,740)The Journal of Organic Chemistry, 1985