化学
光催化
杂原子
芳基
组合化学
表面改性
偶联反应
光化学
催化作用
有机化学
光催化
烷基
物理化学
作者
Indranil Chatterjee,Biprajit Paul,Hrishikesh Paul
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2022-07-14
卷期号:54 (24): 5409-5422
被引量:6
摘要
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
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