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N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions

A new simple, efficient, and environmentally friendly protocol is presented for the catalytic synthesis of α-acyloxycarboxamides using N-formamides as a carbonyl precursor under aqua and mechanochemical conditions. Immobilized sulfuric acid on silica gel was employed for the synthesis of desired pro...

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Autores principales: Salami, Sodeeq Aderotimi, Smith, Vincent J., Krause, Rui W. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890950/
https://www.ncbi.nlm.nih.gov/pubmed/36756572
http://dx.doi.org/10.1039/d2ra06189a
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author Salami, Sodeeq Aderotimi
Smith, Vincent J.
Krause, Rui W. M.
author_facet Salami, Sodeeq Aderotimi
Smith, Vincent J.
Krause, Rui W. M.
author_sort Salami, Sodeeq Aderotimi
collection PubMed
description A new simple, efficient, and environmentally friendly protocol is presented for the catalytic synthesis of α-acyloxycarboxamides using N-formamides as a carbonyl precursor under aqua and mechanochemical conditions. Immobilized sulfuric acid on silica gel was employed for the synthesis of desired products, via the reaction of benzoic acid, 1-napthylisocyanide and various heterocyclic N-formamides. After a careful optimization of the reaction conditions, the desired Passerini products were obtained in high to excellent yields in short reaction times (10–30 min) at room temperature. The highly efficient and environmentally friendly method provides a facile access to a library of α-acyloxycarboxamides derivatives for future research on bioactivity screening.
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spelling pubmed-98909502023-02-07 N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions Salami, Sodeeq Aderotimi Smith, Vincent J. Krause, Rui W. M. RSC Adv Chemistry A new simple, efficient, and environmentally friendly protocol is presented for the catalytic synthesis of α-acyloxycarboxamides using N-formamides as a carbonyl precursor under aqua and mechanochemical conditions. Immobilized sulfuric acid on silica gel was employed for the synthesis of desired products, via the reaction of benzoic acid, 1-napthylisocyanide and various heterocyclic N-formamides. After a careful optimization of the reaction conditions, the desired Passerini products were obtained in high to excellent yields in short reaction times (10–30 min) at room temperature. The highly efficient and environmentally friendly method provides a facile access to a library of α-acyloxycarboxamides derivatives for future research on bioactivity screening. The Royal Society of Chemistry 2023-01-27 /pmc/articles/PMC9890950/ /pubmed/36756572 http://dx.doi.org/10.1039/d2ra06189a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Salami, Sodeeq Aderotimi
Smith, Vincent J.
Krause, Rui W. M.
N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions
title N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions
title_full N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions
title_fullStr N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions
title_full_unstemmed N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions
title_short N-Formamide as a carbonyl precursor in the catalytic synthesis of Passerini adducts under aqua and mechanochemical conditions
title_sort n-formamide as a carbonyl precursor in the catalytic synthesis of passerini adducts under aqua and mechanochemical conditions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890950/
https://www.ncbi.nlm.nih.gov/pubmed/36756572
http://dx.doi.org/10.1039/d2ra06189a
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