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Synlett 1996; 1996(1): 100-102
DOI: 10.1055/s-1996-5335
DOI: 10.1055/s-1996-5335
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Total Synthesis and Absolute Configuration of (-)-Sedacryptine
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
![](https://www.thieme-connect.de/media/synlett/199601/lookinside/thumbnails/10.1055-s-1996-5335-1.jpg)
Enantioselective synthesis of (-)-sedacryptine, a piperidine alkaloid, has been achieved via the double intramolecular conjugate additions or carbamate group and its absolute configuration was determined.
(-)-sedacryptine - piperidine alkaloid - intramolecular conjugate addition - carbamate - absolute configuration