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One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties
The well-known Ugi reaction of aldehydes with amines, carboxylic acids and isocyanides leads to the formation of acyclic α-acylaminocarboxamides. Replacement of the carboxylic acid derivatives with β-acyl substituted acrylic acids gives access to highly substituted 2,5-diketopiperazines in one singl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268348/ https://www.ncbi.nlm.nih.gov/pubmed/23519247 http://dx.doi.org/10.3390/molecules171214685 |
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author | Hartung, Andreas Seufert, Florian Berges, Carsten Gessner, Viktoria H. Holzgrabe, Ulrike |
author_facet | Hartung, Andreas Seufert, Florian Berges, Carsten Gessner, Viktoria H. Holzgrabe, Ulrike |
author_sort | Hartung, Andreas |
collection | PubMed |
description | The well-known Ugi reaction of aldehydes with amines, carboxylic acids and isocyanides leads to the formation of acyclic α-acylaminocarboxamides. Replacement of the carboxylic acid derivatives with β-acyl substituted acrylic acids gives access to highly substituted 2,5-diketopiperazines in one single reaction-step without additives or complex reaction procedures. The obtained diketopiperazines show anti-proliferative effects on activated T cells and represent therefore potential candidates for targeting unwanted T cell-mediated immune responses. |
format | Online Article Text |
id | pubmed-6268348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62683482018-12-14 One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties Hartung, Andreas Seufert, Florian Berges, Carsten Gessner, Viktoria H. Holzgrabe, Ulrike Molecules Article The well-known Ugi reaction of aldehydes with amines, carboxylic acids and isocyanides leads to the formation of acyclic α-acylaminocarboxamides. Replacement of the carboxylic acid derivatives with β-acyl substituted acrylic acids gives access to highly substituted 2,5-diketopiperazines in one single reaction-step without additives or complex reaction procedures. The obtained diketopiperazines show anti-proliferative effects on activated T cells and represent therefore potential candidates for targeting unwanted T cell-mediated immune responses. MDPI 2012-12-11 /pmc/articles/PMC6268348/ /pubmed/23519247 http://dx.doi.org/10.3390/molecules171214685 Text en © 2012 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Hartung, Andreas Seufert, Florian Berges, Carsten Gessner, Viktoria H. Holzgrabe, Ulrike One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties |
title | One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties |
title_full | One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties |
title_fullStr | One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties |
title_full_unstemmed | One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties |
title_short | One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties |
title_sort | one-pot ugi/aza-michael synthesis of highly substituted 2,5-diketopiperazines with anti-proliferative properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268348/ https://www.ncbi.nlm.nih.gov/pubmed/23519247 http://dx.doi.org/10.3390/molecules171214685 |
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