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Acyl Radical Chemistry via Visible-Light Photoredox Catalysis

Open access
Ngai, Ming-Yu, Banerjee, Arghya, Lei, Zhen·2019·Synthesis

Abstract

Visible-light photoredox catalysis enables easy access to acyl radicals under mild reaction conditions. Reactive acyl radicals, generated from various acyl precursors such as aldehydes, α-keto acids, carboxylic acids, anhydrides, acyl thioesters, acyl chlorides, or acyl silanes, can undergo a diverse range of synthetically useful transformations, which were previously difficult or inaccessible. This review summarizes the recent progress on visible-light-driven acyl radical generation using transition-metal photoredox catalysts, metallaphotocatalysts, hypervalent iodine catalysts or organic photocatalysts. 1 Introduction 2 The Scope of This Review 3 Aldehydes as a Source of Acyl Radicals 4 α-Keto Acids as a Source of Acyl Radicals 5 Carboxylic Acids as a Source of Acyl Radicals 6 Anhydrides as a Source of Acyl Radicals 7 Acyl Thioesters as a Source of Acyl Radicals 8 Acyl Chlorides as a Source of Acyl Radicals 9 Acyl Silanes as a Source of Acyl Radicals 10 Conclusions and Future Outlook

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Metadata

Authors
Ngai, M.-Y., Banerjee, A., & Lei, Z.
Venue
Synthesis
Published
2018-12-12
Volume
51
Issue
02
Pages
303-333
ISSN
  • 0039-7881 (ISSN-L)
  • 1437-210X
OpenAlex
W2904940349
Cited by
255
References
1
FWCI
9.77
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Acyl Radical Chemistry via Visible-Light Photoredox Catalysis. https://app.cochat.ai/papers/10.1055/s-0037-1610329
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Ngai, M.-Y., Banerjee, A., & Lei, Z. (2019). Acyl Radical Chemistry via Visible-Light Photoredox Catalysis. Synthesis. https://doi.org/10.1055/s-0037-1610329

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