Issue 27, 2013
From the journal:

RSC Advances

Synthetic studies towards the Lycopodiumalkaloid paniculatine†

Shenghui Lei*a  

* Corresponding authors

a Laboratory of Molecular Engineering, and Laboratory of Natural Product Synthesis, Guangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences, 190 Kaiyuan Avenue, Guangzhou 510530, China
E-mail: lei_shenghui@gibh.ac.cn
Fax: +86-020-32015209
Tel: +86-020-32015336

Abstract

Two bridging tetracyclic products have been observed while attempting to construct the final C-ring of the Lycopodium alkaloid, paniculatine, by an intramolecular addition of enolates to unactivated N-alkyl pyridinium salts.

Graphical abstract: Synthetic studies towards the Lycopodium alkaloid paniculatine

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Article information

DOI
https://doi.org/10.1039/C3RA41467A
Article type
Paper
Submitted
23 Jan 2013
Accepted
17 Apr 2013
First published
18 Apr 2013

RSC Adv., 2013,3, 11014-11020

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Synthetic studies towards the Lycopodium alkaloid paniculatine

S. Lei, RSC Adv., 2013, 3, 11014 DOI: 10.1039/C3RA41467A

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