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Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction

The Suzuki–Miyaura reaction is one of the most used transformations in drug research. Thus making this reaction more sustainable is of considerable current interest. Here we show that propylene carbonate (PC) can be used as a solvent for the Suzuki–Miyaura reaction. PC is one of the greenest solvent...

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Autores principales: Czompa, Andrea, Pásztor, Balázs László, Sahar, Jennifer Alizadeh, Mucsi, Zoltán, Bogdán, Dóra, Ludányi, Krisztina, Varga, Zoltán, Mándity, István M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075783/
https://www.ncbi.nlm.nih.gov/pubmed/35541805
http://dx.doi.org/10.1039/c9ra07044c
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author Czompa, Andrea
Pásztor, Balázs László
Sahar, Jennifer Alizadeh
Mucsi, Zoltán
Bogdán, Dóra
Ludányi, Krisztina
Varga, Zoltán
Mándity, István M.
author_facet Czompa, Andrea
Pásztor, Balázs László
Sahar, Jennifer Alizadeh
Mucsi, Zoltán
Bogdán, Dóra
Ludányi, Krisztina
Varga, Zoltán
Mándity, István M.
author_sort Czompa, Andrea
collection PubMed
description The Suzuki–Miyaura reaction is one of the most used transformations in drug research. Thus making this reaction more sustainable is of considerable current interest. Here we show that propylene carbonate (PC) can be used as a solvent for the Suzuki–Miyaura reaction. PC is one of the greenest solvents since it is synthesized under green conditions by the use of carbon dioxide in the air. All reactions proceeded well and good or excellent yields were observed for the biaryl products. Nonetheless in the case of pyridazinones, 2-hydroxypropyl- chain containing side-products were observed. Importantly, this fact allowed the isolation of several novel compounds which were generated under prominently green conditions.
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spelling pubmed-90757832022-05-09 Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction Czompa, Andrea Pásztor, Balázs László Sahar, Jennifer Alizadeh Mucsi, Zoltán Bogdán, Dóra Ludányi, Krisztina Varga, Zoltán Mándity, István M. RSC Adv Chemistry The Suzuki–Miyaura reaction is one of the most used transformations in drug research. Thus making this reaction more sustainable is of considerable current interest. Here we show that propylene carbonate (PC) can be used as a solvent for the Suzuki–Miyaura reaction. PC is one of the greenest solvents since it is synthesized under green conditions by the use of carbon dioxide in the air. All reactions proceeded well and good or excellent yields were observed for the biaryl products. Nonetheless in the case of pyridazinones, 2-hydroxypropyl- chain containing side-products were observed. Importantly, this fact allowed the isolation of several novel compounds which were generated under prominently green conditions. The Royal Society of Chemistry 2019-11-20 /pmc/articles/PMC9075783/ /pubmed/35541805 http://dx.doi.org/10.1039/c9ra07044c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Czompa, Andrea
Pásztor, Balázs László
Sahar, Jennifer Alizadeh
Mucsi, Zoltán
Bogdán, Dóra
Ludányi, Krisztina
Varga, Zoltán
Mándity, István M.
Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction
title Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction
title_full Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction
title_fullStr Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction
title_full_unstemmed Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction
title_short Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction
title_sort scope and limitation of propylene carbonate as a sustainable solvent in the suzuki–miyaura reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075783/
https://www.ncbi.nlm.nih.gov/pubmed/35541805
http://dx.doi.org/10.1039/c9ra07044c
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