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Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction

A chiral bio-based building block, prepared by the lipase-mediated desymmetrization of an erythritol derivative, was further functionalized and then submitted to stereoselective Passerini reactions, allowing the synthesis of a small library of new molecules. Thanks to the presence of different funct...

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Detalles Bibliográficos
Autores principales: Vitali Forconesi, Gabriella, Banfi, Luca, Basso, Andrea, Lambruschini, Chiara, Moni, Lisa, Riva, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397154/
https://www.ncbi.nlm.nih.gov/pubmed/32679733
http://dx.doi.org/10.3390/molecules25143227
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author Vitali Forconesi, Gabriella
Banfi, Luca
Basso, Andrea
Lambruschini, Chiara
Moni, Lisa
Riva, Renata
author_facet Vitali Forconesi, Gabriella
Banfi, Luca
Basso, Andrea
Lambruschini, Chiara
Moni, Lisa
Riva, Renata
author_sort Vitali Forconesi, Gabriella
collection PubMed
description A chiral bio-based building block, prepared by the lipase-mediated desymmetrization of an erythritol derivative, was further functionalized and then submitted to stereoselective Passerini reactions, allowing the synthesis of a small library of new molecules. Thanks to the presence of different functional groups, further cyclizations were performed providing bicyclic polyoxygenated heterocycles.
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spelling pubmed-73971542020-08-16 Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction Vitali Forconesi, Gabriella Banfi, Luca Basso, Andrea Lambruschini, Chiara Moni, Lisa Riva, Renata Molecules Article A chiral bio-based building block, prepared by the lipase-mediated desymmetrization of an erythritol derivative, was further functionalized and then submitted to stereoselective Passerini reactions, allowing the synthesis of a small library of new molecules. Thanks to the presence of different functional groups, further cyclizations were performed providing bicyclic polyoxygenated heterocycles. MDPI 2020-07-15 /pmc/articles/PMC7397154/ /pubmed/32679733 http://dx.doi.org/10.3390/molecules25143227 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
Vitali Forconesi, Gabriella
Banfi, Luca
Basso, Andrea
Lambruschini, Chiara
Moni, Lisa
Riva, Renata
Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction
title Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction
title_full Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction
title_fullStr Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction
title_full_unstemmed Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction
title_short Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction
title_sort synthesis of polyoxygenated heterocycles by diastereoselective functionalization of a bio-based chiral aldehyde exploiting the passerini reaction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397154/
https://www.ncbi.nlm.nih.gov/pubmed/32679733
http://dx.doi.org/10.3390/molecules25143227
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