Photoredox-Mediated Desulfonylative Radical Reactions: An Excellent Approach Towards C–C and C–Heteroatom Bond Formation

Biprajit Paul; Hrishikesh Paul; Indranil Chatterjee

doi:10.1055/a-1900-8895

Synthesis, Table of Contents

Synthesis 2022; 54(24): 5409-5422
DOI: 10.1055/a-1900-8895

short review

Photoredox-Mediated Desulfonylative Radical Reactions: An Excellent Approach Towards C–C and C–Heteroatom Bond Formation

Authors

Biprajit Paul‡
Hrishikesh Paul‡
Indranil Chatterjee∗

Abstract

All articles of this category

Abstract

In recent times, desulfonylative radical-cross-coupling (RCC) has come to the forefront in synthetic organic, bio, and material chemistry as a powerful strategy to form C–C and C–heteroatom bonds. Diverse functionalization through metal- and photoredox-catalyzed desulfonylation reactions has attracted the scientific community due to the mild reaction conditions, wide functional group tolerance, and excellent synthetic efficacy. In this review, we have highlighted photoredox-mediated desulfonylation reactions developed since 2000. This review will summarize the newly reported methodologies, with particular emphasis on their mechanistic aspects and selectivity issues which have paved a new way towards sustainable C–C and C–X (X = H or heteroatom) bond formation.

1 Introduction

2 Photoredox-Catalyzed C–C Bond Formation

2.1 Aryl Sulfones as Radical Precursor

2.2 Reactions of Allyl Sulfones

3 Photoredox-Catalyzed C–Heteroatom Bond Formation

4 Conclusion

Key words

desulfonylation - radical cross-coupling - photoredox catalysis - C–C bond formation - allyl sulfone

Full Text

References

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