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Versatile Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines
[Image: see text] Herein, we report a convenient synthesis of unprecedented aza-diketopiperazines (aza-DKPs). The strategy is based on selective diversification of bicyclic aza-DKP scaffolds by click reaction, N-acylation, and/or N-alkylation. These scaffolds containing either azido or amino groups...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643515/ https://www.ncbi.nlm.nih.gov/pubmed/31458181 http://dx.doi.org/10.1021/acsomega.8b01752 |
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author | Péron, Florent Riché, Stéphanie Lesur, Brigitte Hibert, Marcel Breton, Philippe Fourquez, Jean-Marie Girard, Nicolas Bonnet, Dominique |
author_facet | Péron, Florent Riché, Stéphanie Lesur, Brigitte Hibert, Marcel Breton, Philippe Fourquez, Jean-Marie Girard, Nicolas Bonnet, Dominique |
author_sort | Péron, Florent |
collection | PubMed |
description | [Image: see text] Herein, we report a convenient synthesis of unprecedented aza-diketopiperazines (aza-DKPs). The strategy is based on selective diversification of bicyclic aza-DKP scaffolds by click reaction, N-acylation, and/or N-alkylation. These scaffolds containing either azido or amino groups were obtained by a key Rh(I)-catalyzed hydroformylative cyclohydrocarbonylation reaction of allyl-substituted aza-DKP. The methodology is readily amenable to the parallel synthesis of original aza-DKPs to enlarge the chemical diversity of aza-heterocycles. |
format | Online Article Text |
id | pubmed-6643515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66435152019-08-27 Versatile Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines Péron, Florent Riché, Stéphanie Lesur, Brigitte Hibert, Marcel Breton, Philippe Fourquez, Jean-Marie Girard, Nicolas Bonnet, Dominique ACS Omega [Image: see text] Herein, we report a convenient synthesis of unprecedented aza-diketopiperazines (aza-DKPs). The strategy is based on selective diversification of bicyclic aza-DKP scaffolds by click reaction, N-acylation, and/or N-alkylation. These scaffolds containing either azido or amino groups were obtained by a key Rh(I)-catalyzed hydroformylative cyclohydrocarbonylation reaction of allyl-substituted aza-DKP. The methodology is readily amenable to the parallel synthesis of original aza-DKPs to enlarge the chemical diversity of aza-heterocycles. American Chemical Society 2018-11-09 /pmc/articles/PMC6643515/ /pubmed/31458181 http://dx.doi.org/10.1021/acsomega.8b01752 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Péron, Florent Riché, Stéphanie Lesur, Brigitte Hibert, Marcel Breton, Philippe Fourquez, Jean-Marie Girard, Nicolas Bonnet, Dominique Versatile Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines |
title | Versatile
Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines |
title_full | Versatile
Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines |
title_fullStr | Versatile
Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines |
title_full_unstemmed | Versatile
Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines |
title_short | Versatile
Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines |
title_sort | versatile
synthetic approach for selective diversification of bicyclic aza-diketopiperazines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643515/ https://www.ncbi.nlm.nih.gov/pubmed/31458181 http://dx.doi.org/10.1021/acsomega.8b01752 |
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