Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates

The purpose of this focus review is to provide a comprehensive overview of the direct synthesis of five-membered cyclic carbonates via oxidative carboxylation of the corresponding olefins and carbon dioxide with particular attention on the mechanistic features of the reactions. The review is divided...

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Autores principales: Wang, Liang, Que, Sisi, Ding, Ziwei, Vessally, Esmail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050038/
https://www.ncbi.nlm.nih.gov/pubmed/35496570
http://dx.doi.org/10.1039/c9ra10755j
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author Wang, Liang
Que, Sisi
Ding, Ziwei
Vessally, Esmail
author_facet Wang, Liang
Que, Sisi
Ding, Ziwei
Vessally, Esmail
author_sort Wang, Liang
collection PubMed
description The purpose of this focus review is to provide a comprehensive overview of the direct synthesis of five-membered cyclic carbonates via oxidative carboxylation of the corresponding olefins and carbon dioxide with particular attention on the mechanistic features of the reactions. The review is divided into two main sections. The first section is a discussion of the single-step reactions, while the second consists of an overview of one-pot, two-step sequential reactions.
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spelling pubmed-90500382022-04-29 Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates Wang, Liang Que, Sisi Ding, Ziwei Vessally, Esmail RSC Adv Chemistry The purpose of this focus review is to provide a comprehensive overview of the direct synthesis of five-membered cyclic carbonates via oxidative carboxylation of the corresponding olefins and carbon dioxide with particular attention on the mechanistic features of the reactions. The review is divided into two main sections. The first section is a discussion of the single-step reactions, while the second consists of an overview of one-pot, two-step sequential reactions. The Royal Society of Chemistry 2020-03-03 /pmc/articles/PMC9050038/ /pubmed/35496570 http://dx.doi.org/10.1039/c9ra10755j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Liang
Que, Sisi
Ding, Ziwei
Vessally, Esmail
Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates
title Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates
title_full Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates
title_fullStr Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates
title_full_unstemmed Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates
title_short Oxidative carboxylation of olefins with CO(2): environmentally benign access to five-membered cyclic carbonates
title_sort oxidative carboxylation of olefins with co(2): environmentally benign access to five-membered cyclic carbonates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050038/
https://www.ncbi.nlm.nih.gov/pubmed/35496570
http://dx.doi.org/10.1039/c9ra10755j
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AT dingziwei oxidativecarboxylationofolefinswithco2environmentallybenignaccesstofivememberedcycliccarbonates
AT vessallyesmail oxidativecarboxylationofolefinswithco2environmentallybenignaccesstofivememberedcycliccarbonates

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