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

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 c...

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Autores principales: Bonandi, Elisa, Tedesco, Giada, Perdicchia, Dario, Passarella, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179133/
https://www.ncbi.nlm.nih.gov/pubmed/32120931
http://dx.doi.org/10.3390/molecules25051057
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author Bonandi, Elisa
Tedesco, Giada
Perdicchia, Dario
Passarella, Daniele
author_facet Bonandi, Elisa
Tedesco, Giada
Perdicchia, Dario
Passarella, Daniele
author_sort Bonandi, Elisa
collection PubMed
description 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 Withania somnifera extract. This natural product was obtained in 9% overall yield over 13 steps, starting from a key homoallylic alcohol previously synthesised in our laboratory. Therefore, the collection of piperidine-derivatives accessible from 2-piperidine ethanol was enriched with a new, diverse scaffold.
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spelling pubmed-71791332020-04-28 Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach Bonandi, Elisa Tedesco, Giada Perdicchia, Dario Passarella, Daniele Molecules Article 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 Withania somnifera extract. This natural product was obtained in 9% overall yield over 13 steps, starting from a key homoallylic alcohol previously synthesised in our laboratory. Therefore, the collection of piperidine-derivatives accessible from 2-piperidine ethanol was enriched with a new, diverse scaffold. MDPI 2020-02-27 /pmc/articles/PMC7179133/ /pubmed/32120931 http://dx.doi.org/10.3390/molecules25051057 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bonandi, Elisa
Tedesco, Giada
Perdicchia, Dario
Passarella, Daniele
Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach
title Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach
title_full Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach
title_fullStr Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach
title_full_unstemmed Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach
title_short Total Synthesis of (–)-Anaferine: A Further Ramification in a Diversity-Oriented Approach
title_sort total synthesis of (–)-anaferine: a further ramification in a diversity-oriented approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179133/
https://www.ncbi.nlm.nih.gov/pubmed/32120931
http://dx.doi.org/10.3390/molecules25051057
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