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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...

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Autores principales: Onwukamike, Kelechukwu Nnabuike, Grelier, Stéphane, Grau, Etienne, Cramail, Henri, Meier, Michael A. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
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.
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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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