Synthese von 7,12‐Dihydro‐indolo[3,2‐d][1]benzazepin‐6‐(5H)‐onen und 6,11‐Dihydro‐thieno‐[3′,2′:2,3]azepino[4,5‐b]indol‐5(4H)‐on
- 1 January 1992
- journal article
- research article
- Published by Wiley in Archiv der Pharmazie
- Vol. 325 (5) , 297-299
- https://doi.org/10.1002/ardp.19923250509
Abstract
Die Titelverbindungen 4 und 6 wurden durch Fischer‐Indol‐Synthese dargestellt. 4a wird durch Brom in Eisessig in 10‐Position substituiert. 4 und 6 zeigen eine schnelle Ringinversion des Azepinringes.Keywords
This publication has 5 references indexed in Scilit:
- Synthese [b]‐kondensierter azepindione durch dealkoxycarbonylierungArchiv der Pharmazie, 1991
- Nuclear magnetic resonance spectroscopy. Application of pulse and Fourier transform carbon-13 nuclear magnetic resonance techniques to structure elucidation. Rauwolfia alkaloidsThe Journal of Organic Chemistry, 1973
- An approach to the synthesis of ibogaineTetrahedron Letters, 1964
- Substitution, Oxidation and Group Participation in the Bromination of IndolesJournal of the American Chemical Society, 1960
- The Alkaloids of Tabernanthe iboga. Part VI.1 The Synthesis of the Selenium Dehydrogenation Products from IbogamineJournal of the American Chemical Society, 1958