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Planta Med 1978; 34(6): 180-182
DOI: 10.1055/s-0028-1097432
DOI: 10.1055/s-0028-1097432
Research Articles
© Georg Thieme Verlag Stuttgart · New York
Stereoselective Reduction of 1–Acetyl–3,4,6,7,12,12b–hexahydroindolo[2,3–a] quinolizine to the Corresponding 1–(1–Hydroxyethyl) Derivative1
1 Synthetic Studies in the Alkaloid Field. Part XI. For part X, see Ref. 11.Further Information
Publication History
Publication Date:
13 January 2009 (online)
![](https://www.thieme-connect.de/media/plantamedica/197806/lookinside/thumbnails/10.1055-s-0028-1097432-1.jpg)
Abstract
The difference in the stereo chemical course of the metal hydride reduction of 3–acetyl–1–,4,6,7,12,12b–hexahydroindolo[2,3–a]quinolizine 1 and 1–acetyl–3,4,6,7,12,12b–hexahydroindolo[2,3–a] quinolizine 4 is described.
Key Word Index
Acetylindolo[2,3–a]quinolizines - Stereoselective reduction - 13C NMR analysis