Total synthesis of ulapualide A, a novel tris-oxazole containing macrolide from the marine nudibranch Hexabranchus sanguineus
- 1 August 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (33) , 6095-6098
- https://doi.org/10.1016/s0040-4039(98)01257-x
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Total Synthesis of Scytophycin CThe Journal of Organic Chemistry, 1997
- Total Synthesis of Aplyronine A, a Potent Antitumor Substance of Marine OriginJournal of the American Chemical Society, 1994
- Aplyronine A, a potent antitumor substance and the congeners aplyronines B and C isolated from the sea hare Aplysia kurodaiJournal of the American Chemical Society, 1993
- Stereochemistry of ulapualides, a new family of tris-oxazole-containing macrolide ionophores from marine nudibranchs. A molecular mechanics studyJournal of Computer-Aided Molecular Design, 1993
- Bioactive marine metabolites. 25. Further kabiramides and halichondramides, cytotoxic macrolides embracing trisoxazole, from the Hexabranchus egg massesThe Journal of Organic Chemistry, 1989
- Mycalolides A – C, hybrid macrolides of ulapualides and halichondramide, from a sponge of the genusTetrahedron Letters, 1989
- Macrocyclic antifungal metabolites from the Spanish dancer nudibranch Hexabranchus sanguineus and sponges of the genus HalichondriaThe Journal of Organic Chemistry, 1988
- Scytophycins, cytotoxic and antimycotic agents from the cyanophyte Scytonema pseudohofmanniThe Journal of Organic Chemistry, 1986
- Bioactive marine metabolites. Part 13. Kabiramide C, a novel antifungal macrolide from nudibranch eggmassesJournal of the American Chemical Society, 1986
- Ulapualide A and B, extraordinary antitumor macrolides from nudibranch eggmassesJournal of the American Chemical Society, 1986