Issue 23, 2021

Recent advances in the incorporation of CO2 for C–H and C–C bond functionalization

Abstract

Carbon dioxide (CO2) has emerged as an exciting, cost-effective, abundant, and ready-to-use C1 source in synthetic organic chemistry. However, the thermodynamic stability and kinetic inertness of CO2 limit its direct fixation, which can only occur in the presence of air-sensitive organometallic reagents, creating a hurdle for its practical utilization in synthetic chemistry. In the past decade, numerous research groups have explored the successful possibility of incorporating CO2 into organic motifs by directly targeting C(sp2)–H, C(sp3)–H, and unsaturated C–C bonds. Furthermore, diverse methods utilizing metal-based redox catalysis, organic and metal-photo-redox catalysis, and metal-free carboxylation methodologies have been developed to achieve CO2-fixation on a wide variety of unsaturated, saturated, and aromatic motifs. This tutorial review aims to aid readers navigate through the development of CO2 functionalization in this particular research area. Additionally, this review also provides an outline for approaching the synthetic challenges, addressing the potential pitfalls, and recognizing the future directions for CO2 utilization. This tutorial review depicts the important aspects of these developments to help readers navigate the vast pool of tactics involving CO2-fixation, leading to valuable moieties that are widely employed in synthetic, pharmaceutical, material, and bio industries.

Graphical abstract: Recent advances in the incorporation of CO2 for C–H and C–C bond functionalization

Article information

Article type
Tutorial Review
Submitted
31 Jul 2021
Accepted
22 Okt 2021
First published
22 Okt 2021

Green Chem., 2021,23, 9283-9317

Recent advances in the incorporation of CO2 for C–H and C–C bond functionalization

S. Pimparkar, A. K. Dalvi, A. Koodan, S. Maiti, S. A. Al-Thabaiti, M. Mokhtar, A. Dutta, Y. R. Lee and D. Maiti, Green Chem., 2021, 23, 9283 DOI: 10.1039/D1GC02737A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements