The chemistry of vicinal tricarbonyl compounds. Short syntheses of eudistomins T, I and M
- 1 January 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (50) , 7117-7120
- https://doi.org/10.1016/s0040-4039(01)93439-2
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- The chemistry of vicinal tricarbonyl compounds. Applications in the synthesis of isoquinoline alkaloidsTetrahedron Letters, 1989
- The improved synthesis of 7-oxygenated indoles by Fischer indolization and its application to the first total synthesis of eudistomidin-ATetrahedron Letters, 1989
- Total synthesis of (-)-eudistomin L and (-)-debromoeudistomin LJournal of the American Chemical Society, 1989
- Short, efficient syntheses of the antibiotic eudistomins I and TTetrahedron Letters, 1989
- The chemistry of vicinal tricarbonyl compounds. Applications in the synthesis of vincamine-related alkaloidsTetrahedron Letters, 1989
- Synthesis of N(10)-acetyleudistomin LTetrahedron Letters, 1989
- The chemistry of vicinal tricarbonyls. A stable vinyl tricarbonyl hydrate as a di- and trielectrophileJournal of the American Chemical Society, 1989
- Three new β-carbolines from the bermudian tunicate Eudistoma olivaceumTetrahedron Letters, 1987
- Eudistomins A, D, G, H, I, J, M, N, O, P, and Q, bromo, hydroxy, pyrrolyl and iminoazepino .beta.-carbolines from the antiviral Caribbean tunicate Eudistoma olivaceumJournal of the American Chemical Society, 1984
- Eudistomins C, E, K, and L, potent antiviral compounds containing a novel oxathiazepine ring from the Caribbean tunicate Eudistoma olivaceumJournal of the American Chemical Society, 1984