Total Synthesis of (-)-Anaferine: A Further Ramification in a Diversity-Oriented Approach.


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
27 Feb 2020
Historique:
received: 10 02 2020
revised: 24 02 2020
accepted: 26 02 2020
entrez: 4 3 2020
pubmed: 4 3 2020
medline: 14 1 2021
Statut: epublish

Résumé

The piperidine ring is a widespread motif in several natural bioactive alkaloids of both vegetal and marine origin. In the last years, a diversity-oriented synthetic (DOS) approach, aimed at the generation of a library of piperidine-based derivatives, was developed in our research group, employing commercially available 2-piperidine ethanol as a versatile precursor. Here, we report the exploration of another ramification of our DOS approach, that led us to the stereoselective total synthesis of (-)-anaferine, a bis-piperidine alkaloid present in

Identifiants

pubmed: 32120931
pii: molecules25051057
doi: 10.3390/molecules25051057
pmc: PMC7179133
pii:
doi:

Substances chimiques

Alkaloids 0
Piperidines 0
Plant Extracts 0
Ethanol 3K9958V90M
piperidine 67I85E138Y

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

Chempluschem. 2019 Jan;84(1):98-102
pubmed: 31950734
J Org Chem. 2008 Jun 6;73(11):4225-8
pubmed: 18459814
Cell Mol Life Sci. 2015 Dec;72(23):4445-60
pubmed: 26306935
Med Hypotheses. 2016 Jul;92:35-43
pubmed: 27241252
Org Biomol Chem. 2012 Jan 7;10(1):154-61
pubmed: 22068547
Eur J Med Chem. 2015 Mar 6;92:766-75
pubmed: 25626146
J Org Chem. 2010 Apr 16;75(8):2610-8
pubmed: 20230016
Org Lett. 2001 Jan 25;3(2):193-6
pubmed: 11430032
J Org Chem. 2009 Oct 2;74(19):7417-28
pubmed: 19739615
Food Chem Toxicol. 2012 Jun;50(6):2049-55
pubmed: 22449544
Neurotoxicol Teratol. 2010 May-Jun;32(3):383-90
pubmed: 20116429
Bioorg Med Chem Lett. 2010 Oct 1;20(19):5905-8
pubmed: 20727745
Int J Mol Sci. 2015 Dec 24;17(1):
pubmed: 26712740
J Nat Prod. 2004 Oct;67(10):1758-60
pubmed: 15497958
Mar Drugs. 2019 Aug 15;17(8):
pubmed: 31443260
J Nat Prod. 2007 Apr;70(4):538-43
pubmed: 17346073
Chemistry. 2011 May 23;17(22):6221-6
pubmed: 21506188

Auteurs

Elisa Bonandi (E)

Università degli Studi di Milano, Via Golgi 19, 20133 Milano, Italy.

Giada Tedesco (G)

Università degli Studi di Milano, Via Golgi 19, 20133 Milano, Italy.

Dario Perdicchia (D)

Università degli Studi di Milano, Via Golgi 19, 20133 Milano, Italy.

Daniele Passarella (D)

Università degli Studi di Milano, Via Golgi 19, 20133 Milano, Italy.

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Classifications MeSH