Reaktionen an Indolderivaten, XIII. Chinolon‐Derivate durch Autoxydation
- 30 April 1971
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 745 (1) , 23-30
- https://doi.org/10.1002/jlac.19717450105
Abstract
2.3‐Disubstituierte Indol‐Verbindungen vom Tetrahydroharman‐Typ (5, 21, 24, 25) werden in Dimethylformamid mit Kalium‐tert.‐butylat und Sauerstoff in Chinolone (6, 22, 23, 26, 27) übergeführt. Die Bedeutung dieser Reaktion für die Biogenese des Camptothecins (1) wird diskutiert.Keywords
This publication has 18 references indexed in Scilit:
- Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata1,2Journal of the American Chemical Society, 1966
- The Periodate Oxidation of Indoles1Journal of the American Chemical Society, 1966
- Chemiluminescence of indolyl peroxidesChemical Communications (London), 1966
- Oxidative Transformations of Indole Alkaloids. III. Pseudoindoxyls from Yohimbinoid Alkaloids and Their Conversion to “Invert” Alkaloids1,2Journal of the American Chemical Society, 1965
- Mass Spectrometry in Structural and Stereochemical Problems. XLVII.1Some Observations on Mass Spectra of Pseudoindoxyl Alkaloids2Journal of the American Chemical Society, 1964
- The Autoöxidation of 2,3-Diethylindole to 2-Acetyl-3-ethylindole1Journal of the American Chemical Society, 1961
- Peroxides of tetrahydrocarbazole and related compounds. Part VI. Some indoleninyl hydroperoxidesJournal of the Chemical Society, 1954
- The Conversion of Tetrahydroharman Alkaloids into Derivatives of Linear Pyrroquinolones1Journal of the American Chemical Society, 1953
- Ring Effects in Autoxidation. A New Type of Camps Reaction1,2Journal of the American Chemical Society, 1951
- 638. Peroxides of tetrahydrocarbazole and related compounds. Part IIJournal of the Chemical Society, 1950