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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...

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Autores principales: Péron, Florent, Riché, Stéphanie, Lesur, Brigitte, Hibert, Marcel, Breton, Philippe, Fourquez, Jean-Marie, Girard, Nicolas, Bonnet, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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