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Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling

The development of new and greener approaches to organic synthesis has been a trend in recent years. Continuing the latest publications of our team, in this work, we demonstrate the efficiency of three solvents: eucalyptol (1,8-cineole), cyclopentyl methyl ether (CPME), and 2-methyltetrahydrofuran (...

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Autores principales: Campos, Joana F., Cailler, Manon, Claudel, Remi, Prot, Benjamin, Besson, Thierry, Berteina-Raboin, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922032/
https://www.ncbi.nlm.nih.gov/pubmed/33670633
http://dx.doi.org/10.3390/molecules26041074
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author Campos, Joana F.
Cailler, Manon
Claudel, Remi
Prot, Benjamin
Besson, Thierry
Berteina-Raboin, Sabine
author_facet Campos, Joana F.
Cailler, Manon
Claudel, Remi
Prot, Benjamin
Besson, Thierry
Berteina-Raboin, Sabine
author_sort Campos, Joana F.
collection PubMed
description The development of new and greener approaches to organic synthesis has been a trend in recent years. Continuing the latest publications of our team, in this work, we demonstrate the efficiency of three solvents: eucalyptol (1,8-cineole), cyclopentyl methyl ether (CPME), and 2-methyltetrahydrofuran (2-MeTHF) for the synthesis of O,S,N-heterocyclic compounds.
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spelling pubmed-79220322021-03-03 Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling Campos, Joana F. Cailler, Manon Claudel, Remi Prot, Benjamin Besson, Thierry Berteina-Raboin, Sabine Molecules Article The development of new and greener approaches to organic synthesis has been a trend in recent years. Continuing the latest publications of our team, in this work, we demonstrate the efficiency of three solvents: eucalyptol (1,8-cineole), cyclopentyl methyl ether (CPME), and 2-methyltetrahydrofuran (2-MeTHF) for the synthesis of O,S,N-heterocyclic compounds. MDPI 2021-02-18 /pmc/articles/PMC7922032/ /pubmed/33670633 http://dx.doi.org/10.3390/molecules26041074 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Campos, Joana F.
Cailler, Manon
Claudel, Remi
Prot, Benjamin
Besson, Thierry
Berteina-Raboin, Sabine
Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
title Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
title_full Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
title_fullStr Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
title_full_unstemmed Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
title_short Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
title_sort demonstration of green solvent performance on o,s,n-heterocycles synthesis: metal-free click chemistry and buchwald—hartwig coupling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922032/
https://www.ncbi.nlm.nih.gov/pubmed/33670633
http://dx.doi.org/10.3390/molecules26041074
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