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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...

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Detalles Bibliográficos
Autores principales: Hartung, Andreas, Seufert, Florian, Berges, Carsten, Gessner, Viktoria H., Holzgrabe, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
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.
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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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