Abstract
Treatment of piperidine 8 with acetyl chloride or ethyl chloroformate in the presence of triethylamine gave the 2,3-dehydrogenated products 10a and 10b, respectively, together with the expected N-acylpiperidines 9.
Keywords: N-acyl adamantylmethylpiperidines, N-acyl adamantylmethyltetrahydropiperidines, synthesis
Letters in Organic Chemistry
Title: An Intriguing, Regioselective Synthesis of Novel 2-(1-Adamantylmethyl) tetrahydropyridines
Volume: 5 Issue: 1
Author(s): George B. Foscolos, Ioannis Papanastasiou and Andrew Tsotinis
Affiliation:
Keywords: N-acyl adamantylmethylpiperidines, N-acyl adamantylmethyltetrahydropiperidines, synthesis
Abstract: Treatment of piperidine 8 with acetyl chloride or ethyl chloroformate in the presence of triethylamine gave the 2,3-dehydrogenated products 10a and 10b, respectively, together with the expected N-acylpiperidines 9.
Export Options
About this article
Cite this article as:
Foscolos B. George, Papanastasiou Ioannis and Tsotinis Andrew, An Intriguing, Regioselective Synthesis of Novel 2-(1-Adamantylmethyl) tetrahydropyridines, Letters in Organic Chemistry 2008; 5 (1) . https://dx.doi.org/10.2174/157017808783330117
DOI https://dx.doi.org/10.2174/157017808783330117 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers