Issue 1, 2023

Eosin Y mediated photo-catalytic C–H functionalization: C–C and C–S bond formation

Abstract

C–C and C–S bonds are valuable in organic transformation for synthesizing various bioactive heterocycles. Owing to the increasing awareness of the step and atom economy of a reaction, organic chemists have promulgated the idea of sustainable and green chemistry for organic synthesis. Hence, photoredox catalysis using organic dyes as photocatalysts has attracted constant attention over the last decade. Herein, recent advances and developments (over the previous ten years, 2012–2022) in eosin Y mediated photoredox catalyzed synthetic organic transformations for C–C and C–S bond formation along with their different mechanistic pathways (such as SET, HAT, and energy transfer) are discussed. This review is classified into two major sections, (i) C–C and (ii) C–S bond formations, which are further sub-categorized into various types of functionalizations including arylation, alkenylation, annulation, thionation, and sulfonylation.

Graphical abstract: Eosin Y mediated photo-catalytic C–H functionalization: C–C and C–S bond formation

Article information

Article type
Review Article
Submitted
28 sep 2022
Accepted
22 nov 2022
First published
23 nov 2022

Org. Chem. Front., 2023,10, 237-266

Eosin Y mediated photo-catalytic C–H functionalization: C–C and C–S bond formation

D. Singla, V. Luxami and K. Paul, Org. Chem. Front., 2023, 10, 237 DOI: 10.1039/D2QO01534J

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