Unknown

Dataset Information

0

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


ABSTRACT: 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.

SUBMITTER: Bonandi E 

PROVIDER: S-EPMC7179133 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

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

Bonandi Elisa E   Tedesco Giada G   Perdicchia Dario D   Passarella Daniele D  

Molecules (Basel, Switzerland) 20200227 5


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  ...[more]

Similar Datasets

| S-EPMC3359144 | biostudies-literature
| S-EPMC3252850 | biostudies-literature
| S-EPMC8162117 | biostudies-literature
| S-EPMC3084124 | biostudies-literature
| S-EPMC7214869 | biostudies-literature
| S-EPMC6282055 | biostudies-literature
| S-EPMC3099625 | biostudies-literature
| S-EPMC5515376 | biostudies-literature
| S-EPMC7709968 | biostudies-literature