Issue 12, 2020

Transition metal-catalyzed coupling of heterocyclic alkenes via C–H functionalization: recent trends and applications

Abstract

Heterocyclic alkenes represent an important class of reactive feedstock and valuable synthons for the synthesis of biologically important heterocyclic scaffolds. Although functionalized heterocyclic alkenes and their derivatives can be accessed via metal-catalyzed cross-coupling reactions, yet the prefunctionalisation of starting materials makes the process a bit cumbersome. On the other hand, transition-metal-catalyzed C–H functionalization is one of the most persuasive and front-line research areas in modern synthetic organic chemistry for atom/step-economy, viability and high efficacy. This critical review highlights the recent advances in coupling of heterocyclic alkenes by transition-metal-catalyzed reactions with special emphasis on arylation, alkenylation, alkylation, hydroarylation, ring-opening addition and annulation/cyclization via the C–H functionalization strategy reported since 2015.

Graphical abstract: Transition metal-catalyzed coupling of heterocyclic alkenes via C–H functionalization: recent trends and applications

Article information

Article type
Review Article
Submitted
09 Нау. 2020
Accepted
28 Сәу. 2020
First published
29 Сәу. 2020

Org. Chem. Front., 2020,7, 1527-1569

Transition metal-catalyzed coupling of heterocyclic alkenes via C–H functionalization: recent trends and applications

S. Vivek Kumar, S. Banerjee and T. Punniyamurthy, Org. Chem. Front., 2020, 7, 1527 DOI: 10.1039/D0QO00279H

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