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Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry
For almost 20 years, thioureas have been experiencing a renaissance of interest with the emerged development of asymmetric organocatalysts. Due to their relatively high acidity and strong hydrogen bond donor capability, they differ significantly from ureas and offer, appropriately modified, great po...
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/PMC7024223/ https://www.ncbi.nlm.nih.gov/pubmed/31963671 http://dx.doi.org/10.3390/molecules25020401 |
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author | Steppeler, Franz Iwan, Dominika Wojaczyńska, Elżbieta Wojaczyński, Jacek |
author_facet | Steppeler, Franz Iwan, Dominika Wojaczyńska, Elżbieta Wojaczyński, Jacek |
author_sort | Steppeler, Franz |
collection | PubMed |
description | For almost 20 years, thioureas have been experiencing a renaissance of interest with the emerged development of asymmetric organocatalysts. Due to their relatively high acidity and strong hydrogen bond donor capability, they differ significantly from ureas and offer, appropriately modified, great potential as organocatalysts, chelators, drug candidates, etc. The review focuses on the family of chiral thioureas, presenting an overview of the current state of knowledge on their synthesis and selected applications in stereoselective synthesis and drug development. |
format | Online Article Text |
id | pubmed-7024223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70242232020-03-19 Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry Steppeler, Franz Iwan, Dominika Wojaczyńska, Elżbieta Wojaczyński, Jacek Molecules Review For almost 20 years, thioureas have been experiencing a renaissance of interest with the emerged development of asymmetric organocatalysts. Due to their relatively high acidity and strong hydrogen bond donor capability, they differ significantly from ureas and offer, appropriately modified, great potential as organocatalysts, chelators, drug candidates, etc. The review focuses on the family of chiral thioureas, presenting an overview of the current state of knowledge on their synthesis and selected applications in stereoselective synthesis and drug development. MDPI 2020-01-18 /pmc/articles/PMC7024223/ /pubmed/31963671 http://dx.doi.org/10.3390/molecules25020401 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 | Review Steppeler, Franz Iwan, Dominika Wojaczyńska, Elżbieta Wojaczyński, Jacek Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry |
title | Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry |
title_full | Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry |
title_fullStr | Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry |
title_full_unstemmed | Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry |
title_short | Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry |
title_sort | chiral thioureas—preparation and significance in asymmetric synthesis and medicinal chemistry |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024223/ https://www.ncbi.nlm.nih.gov/pubmed/31963671 http://dx.doi.org/10.3390/molecules25020401 |
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