Issue 15, 2020
From the journal:

RSC Advances

Oxidative carboxylation of olefins with CO2: environmentally benign access to five-membered cyclic carbonates

Liang Wang,a   Sisi Que,abc   Ziwei Dingb  and  Esmail Vessally ORCID logo *d  

* Corresponding authors

a State Key Lab of Coal Mine Disaster Dynamics and Control, Chongqing University, Chongqing 400044, China

b State Key Laboratory of Coal Resources in Western China, Xi'an University of Science and Technology, Xi'an, China

c Key Laboratory of Hydraulic and Waterway Engineering of the Ministry of Education, College of River and Ocean Engineering, Chongqing Jiaotong University, Chongqing 400074, China

d Department of Chemistry, Payame Noor University, Tehran, Iran
E-mail: vessally@yahoo.com, vesali@pnu.ac.ir

Abstract

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.

Graphical abstract: Oxidative carboxylation of olefins with CO2: environmentally benign access to five-membered cyclic carbonates

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Article information

DOI
https://doi.org/10.1039/C9RA10755J
Article type
Review Article
Submitted
20 Dec 2019
Accepted
18 Feb 2020
First published
03 Mar 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 9103-9115

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Oxidative carboxylation of olefins with CO2: environmentally benign access to five-membered cyclic carbonates

L. Wang, S. Que, Z. Ding and E. Vessally, RSC Adv., 2020, 10, 9103 DOI: 10.1039/C9RA10755J

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