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On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction
We introduce a novel isocyanide-based multicomponent reaction, the Passerini four component reaction (P-4CR), by replacing the carboxylic acid component of a conventional Passerini three component reaction (P-3CR) with an alcohol and CO(2). Key to this approach is the use of a switchable solvent sys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085615/ https://www.ncbi.nlm.nih.gov/pubmed/35548239 http://dx.doi.org/10.1039/c8ra07150k |
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author | Onwukamike, Kelechukwu Nnabuike Grelier, Stéphane Grau, Etienne Cramail, Henri Meier, Michael A. R. |
author_facet | Onwukamike, Kelechukwu Nnabuike Grelier, Stéphane Grau, Etienne Cramail, Henri Meier, Michael A. R. |
author_sort | Onwukamike, Kelechukwu Nnabuike |
collection | PubMed |
description | We introduce a novel isocyanide-based multicomponent reaction, the Passerini four component reaction (P-4CR), by replacing the carboxylic acid component of a conventional Passerini three component reaction (P-3CR) with an alcohol and CO(2). Key to this approach is the use of a switchable solvent system, allowing the synthesis of a variety of α-carbonate-amides. The reaction was first investigated and optimized using butanol, isobutyraldehyde, tert-butyl isocyanide and CO(2). Parameters investigated included the effect of reactant equivalents, reactant concentration, solvent, catalyst, catalyst concentration and CO(2) pressure. Of the other parameters, the purity of the aldehyde and its tendency to oxidize was one of the most critical parameters for a successful P-4CR. After optimization, a total of twelve (12) P-4CR compounds were synthesized with conversions ranging between 16 and 82% and isolated yields between 18 and 43%. Their structures were confirmed via(1)H and (13)C NMR, FT-IR and high resolution mass spectrometry (ESI-MS). In addition, three (3) hydrolysis products of P-4CR (α-hydroxyl-amides) were successfully isolated with yields between 23 and 63% and fully characterized ((1)H, (13)C NMR, FT-IR and ESI-MS) as well. |
format | Online Article Text |
id | pubmed-9085615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90856152022-05-10 On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction Onwukamike, Kelechukwu Nnabuike Grelier, Stéphane Grau, Etienne Cramail, Henri Meier, Michael A. R. RSC Adv Chemistry We introduce a novel isocyanide-based multicomponent reaction, the Passerini four component reaction (P-4CR), by replacing the carboxylic acid component of a conventional Passerini three component reaction (P-3CR) with an alcohol and CO(2). Key to this approach is the use of a switchable solvent system, allowing the synthesis of a variety of α-carbonate-amides. The reaction was first investigated and optimized using butanol, isobutyraldehyde, tert-butyl isocyanide and CO(2). Parameters investigated included the effect of reactant equivalents, reactant concentration, solvent, catalyst, catalyst concentration and CO(2) pressure. Of the other parameters, the purity of the aldehyde and its tendency to oxidize was one of the most critical parameters for a successful P-4CR. After optimization, a total of twelve (12) P-4CR compounds were synthesized with conversions ranging between 16 and 82% and isolated yields between 18 and 43%. Their structures were confirmed via(1)H and (13)C NMR, FT-IR and high resolution mass spectrometry (ESI-MS). In addition, three (3) hydrolysis products of P-4CR (α-hydroxyl-amides) were successfully isolated with yields between 23 and 63% and fully characterized ((1)H, (13)C NMR, FT-IR and ESI-MS) as well. The Royal Society of Chemistry 2018-09-07 /pmc/articles/PMC9085615/ /pubmed/35548239 http://dx.doi.org/10.1039/c8ra07150k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Onwukamike, Kelechukwu Nnabuike Grelier, Stéphane Grau, Etienne Cramail, Henri Meier, Michael A. R. On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction |
title | On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction |
title_full | On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction |
title_fullStr | On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction |
title_full_unstemmed | On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction |
title_short | On the direct use of CO(2) in multicomponent reactions: introducing the Passerini four component reaction |
title_sort | on the direct use of co(2) in multicomponent reactions: introducing the passerini four component reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085615/ https://www.ncbi.nlm.nih.gov/pubmed/35548239 http://dx.doi.org/10.1039/c8ra07150k |
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