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Stereoselective Synthesis of Piperidine Alkaloid (+)‐α‐Conhydrine and Its Pyrrolidine Analogue

Stereoselective Synthesis of Piperidine Alkaloid (+)‐α‐Conhydrine and Its Pyrrolidine Analogue Concise stereoselective syntheses of (+)‐α‐conhydrine and its pyrrolidine analogue are described. The key features are a highly diastereoselective chelation‐controlled hydride reduction of the amino ketone, to give the anti amino alcohol directly, and an intramolecular ring‐closing metathesis. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Stereoselective Synthesis of Piperidine Alkaloid (+)‐α‐Conhydrine and Its Pyrrolidine Analogue

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References (59)

Publisher
Wiley
Copyright
Copyright © 2012 Wiley Subscription Services, Inc., A Wiley Company
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201200065
Publisher site
See Article on Publisher Site

Abstract

Concise stereoselective syntheses of (+)‐α‐conhydrine and its pyrrolidine analogue are described. The key features are a highly diastereoselective chelation‐controlled hydride reduction of the amino ketone, to give the anti amino alcohol directly, and an intramolecular ring‐closing metathesis.

Journal

Asian Journal of Organic ChemistryWiley

Published: Nov 1, 2012

Keywords: ; ; ; ;

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