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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7397154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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