A new approach to the synthesis of lavendamycin analogues.
- 1 April 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (18) , 2937-2940
- https://doi.org/10.1016/s0040-4039(00)60486-0
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Connection between metalation and cross-coupling strategies. A new convergent route to azacarbazoles.Tetrahedron, 1993
- Palladium-catalyzed inter- and intramolecular cross-coupling reactions of B-alkyl-9-borabicyclo[3.3.1]nonane derivatives with 1-halo-1-alkenes or haloarenes. Syntheses of functionalized alkenes, arenes, and cycloalkenes via a hydroboration-coupling sequenceJournal of the American Chemical Society, 1989
- Synthesis of lavendamycinTetrahedron, 1986
- A Simple and Regioselective Preparation of 2- or 3-Substituted Quinoline Derivatives via DialkylquinolylboranesHETEROCYCLES, 1985
- Palladium (O) mediated β-carboline synthesis: Preparation of the CDE ring system of lavendamycinTetrahedron Letters, 1984
- The regiospecific total synthesis of lavendamycin methyl esterTetrahedron Letters, 1984
- New Tactics in Heterocycles SynthesisHETEROCYCLES, 1984
- Synthetic Approach to the Antitumor Antibiotic Lavendamycin: a Synthesis of Demethallavendamycin Methyl EsterHETEROCYCLES, 1983
- Structure determination of lavendamycin- a new antitumor antibiotic from streptomyces lavendulaeTetrahedron Letters, 1981
- The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of BasesSynthetic Communications, 1981