Synthesis of dihydro-1-pyrrolo-and tetrahydropyrido[1,2-] indoles via a modified madelung reaction
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 42 (18) , 5053-5064
- https://doi.org/10.1016/s0040-4020(01)88057-1
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Synthesis of mitomycin C analogs. 2. Introduction of a leaving group at C-1 and oxidation of the aromatic ring in 2,3,9,9a-tetrahydro-1H-pyrrolo[1,2-a]indolesThe Journal of Organic Chemistry, 1985
- Synthesis of mitomycin C analogs. 1. Introduction of the urethane function at C-10 of the pyrrolo[1,2-a]indole skeletonThe Journal of Organic Chemistry, 1985
- Synthesis and biological activity of 6-substituted mitosene analogs of the mitomycinsJournal of Medicinal Chemistry, 1985
- Une nouvelle voie d’acces aux indoles par condensation ylure-amideTetrahedron, 1985
- A new versatile synthesis of 4-nitroindolesTetrahedron Letters, 1983
- Lithiation of N-(2-alkylphenyl)alkanamides and related compounds. A modified Madelung indole synthesisThe Journal of Organic Chemistry, 1981
- Synthetic Studies on Mitomycins and Related CompoundsHETEROCYCLES, 1979
- Synthesis and Biological Activities of Mitomycin DerivativesHETEROCYCLES, 1979
- Isolation of crystalline keto-enol tautomers. Conversion into indoles and oxindolesJournal of the American Chemical Society, 1968
- Über eine neue Darstellungsweise für substituierte Indole. IEuropean Journal of Inorganic Chemistry, 1912