Abstract
This review relates a new access to the piperidine ring by intramolecular cyclization of acyl iminium and iminium ions substituted by an allylsilyl side chain as an internal Π-nucleophile. This methodology was applied to the synthesis of piperidine alkaloids
Keywords: Piperidine, iminium ions, N-acyliminium ions, indolizidine, quinolizidine
Mini-Reviews in Organic Chemistry
Title: A Convenient Access to the Piperidine Ring by Cyclization of Allylsilyl Substituted N- cyliminium and Iminium Ions: Application to the Synthesis of Piperidine Alkaloids.
Volume: 5 Issue: 3
Author(s): R. Remuson and Y. Gelas-Mialhe
Affiliation:
Keywords: Piperidine, iminium ions, N-acyliminium ions, indolizidine, quinolizidine
Abstract: This review relates a new access to the piperidine ring by intramolecular cyclization of acyl iminium and iminium ions substituted by an allylsilyl side chain as an internal Π-nucleophile. This methodology was applied to the synthesis of piperidine alkaloids
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Cite this article as:
Remuson R. and Gelas-Mialhe Y., A Convenient Access to the Piperidine Ring by Cyclization of Allylsilyl Substituted N- cyliminium and Iminium Ions: Application to the Synthesis of Piperidine Alkaloids., Mini-Reviews in Organic Chemistry 2008; 5 (3) . https://dx.doi.org/10.2174/157019308785161701
DOI https://dx.doi.org/10.2174/157019308785161701 |
Print ISSN 1570-193X |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6298 |
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