Visible light-mediated halogenation of organic compounds

Alexey A. Festa; Olga A. Storozhenko; Leonid G. Voskressensky; Erik V. Van der Eycken

doi:10.1039/d3cs00366c

journal article Open Access Jan 01, 2023

Visible light-mediated halogenation of organic compounds

Alexey A. Festa

Olga A. Storozhenko Leonid G. Voskressensky

Erik V. Van der Eycken

Chemical Society Reviews Vol. 52 No. 24 pp. 8678-8698 · Royal Society of Chemistry (RSC)

View at Publisher Save 10.1039/d3cs00366c

Abstract

The impact of visible light-promoted chemistry on the halogenation of organic compounds is reviewed.

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References

130

[1]

Benedetto Tiz Molecules (2022) 10.3390/molecules27051643

[2]

Malykhin Adv. Synth. Catal. (2021) 10.1002/adsc.202100284

[3]

Hernandes Curr. Drug Targets (2010) 10.2174/138945010790711996

[4]

Jeschke Pest Manage. Sci. (2010) 10.1002/ps.1829

[5]

Berger Chem. Commun. (2020) 10.1039/d0cc00841a

[6]

Tang Chem. Mater. (2011) 10.1021/cm102182x

[7]

Nicewicz Science (2008) 10.1126/science.1161976

[8]

Ischay J. Am. Chem. Soc. (2008) 10.1021/ja805387f

[9]

Photoredox-Catalyzed C–H Functionalization Reactions

Natalie Holmberg-Douglas, David A. Nicewicz

Chemical Reviews 2022 10.1021/acs.chemrev.1c00311

[10]

Prier Chem. Rev. (2013) 10.1021/cr300503r

[11]

Xuan Angew. Chem., Int. Ed. (2012) 10.1002/anie.201200223

[12]

Chen Chem. Soc. Rev. (2016) 10.1039/c5cs00655d

[13]

Xia J. Am. Chem. Soc. (2013) 10.1021/ja410815u

[14]

Xiang Org. Lett. (2017) 10.1021/acs.orglett.7b01270

[15]

Bume Tetrahedron (2016) 10.1016/j.tet.2016.08.018

[16]

Article Chem. Sci. (2017) 10.1039/c7sc02703f

[17]

Bume J. Org. Chem. (2018) 10.1021/acs.joc.7b02807

[18]

Nobile Angew. Chem., Int. Ed. (2021) 10.1002/anie.202009995

[19]

Dauncey Angew. Chem., Int. Ed. (2018) 10.1002/anie.201710790

[20]

Morcillo Angew. Chem., Int. Ed. (2018) 10.1002/anie.201807941

[21]

Bafaluy Angew. Chem., Int. Ed. (2020) 10.1002/anie.202004902

[22]

Deng Org. Lett. (2021) 10.1021/acs.orglett.1c01020

[23]

Herron J. Am. Chem. Soc. (2020) 10.1021/jacs.9b13171

[24]

Xia Chem. Commun. (2014) 10.1039/c4cc05650g

[25]

Halperin Angew. Chem., Int. Ed. (2014) 10.1002/anie.201400420

[26]

Bloom Chem. Sci. (2014) 10.1039/c3sc53261e

[27]

Kee Chem. Commun. (2014) 10.1039/c4cc01848f

[28]

West Angew. Chem., Int. Ed. (2016) 10.1002/anie.201603149

[29]

Wu Angew. Chem., Int. Ed. (2018) 10.1002/anie.201806554

[30]

Zhang Inorg. Chem. (2020) 10.1021/acs.inorgchem.0c00850

[31]

Wilger Nat. Chem. (2014) 10.1038/nchem.2000

[32]

Deng Org. Lett. (2018) 10.1021/acs.orglett.8b01658

[33]

Zou Org. Biomol. Chem. (2022) 10.1039/d2ob00488g

[34]

Sim ACS Catal. (2019) 10.1021/acscatal.8b04284

[35]

Tang Angew. Chem., Int. Ed. (2020) 10.1002/anie.201916471

[36]

Ohkubo Res. Chem. Intermed. (2013) 10.1007/s11164-012-0643-5

[37]

Chen Science (2019) 10.1126/science.aav7019

[38]

Wang Org. Lett. (2020) 10.1021/acs.orglett.0c02815

[39]

Hu iScience (2020) 10.1016/j.isci.2020.101266

[40]

Zeng Adv. Synth. Catal. (2021) 10.1002/adsc.202100211

[41]

Rueda-Becerril J. Am. Chem. Soc. (2014) 10.1021/ja412083f

[42]

Ventre J. Am. Chem. Soc. (2015) 10.1021/jacs.5b02244

[43]

Wu Chem. Commun. (2015) 10.1039/c5cc04527d

[44]

Webb J. Am. Chem. Soc. (2020) 10.1021/jacs.0c03125

[45]

Xu J. Am. Chem. Soc. (2021) 10.1021/jacs.1c02490

[46]

Chen J. Am. Chem. Soc. (2022) 10.1021/jacs.2c02392

[47]

Zhang Org. Lett. (2022) 10.1021/acs.orglett.2c02242

[48]

Mcteague Angew. Chem., Int. Ed. (2016) 10.1002/anie.201608792

[49]

Mir Tetrahedron (2023) 10.1016/j.tet.2023.133494

[50]

Xiang J. Org. Chem. (2020) 10.1021/acs.joc.0c01000

Showing 50 of 130 references

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Metrics

53

Citations

130

References

Details

Published: Jan 01, 2023
Vol/Issue: 52(24)
Pages: 8678-8698
License: View

Authors

A

Alexey A. Festa

Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya st. 6, Moscow, 117198, Russian Federation

O

Olga A. Storozhenko

Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya st. 6, Moscow, 117198, Russian Federation

L

Leonid G. Voskressensky

Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya st. 6, Moscow, 117198, Russian Federation

E

Erik V. Van der Eycken

Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya st. 6, Moscow, 117198, Russian Federation; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, B-3001, Leuven, Belgium

Funding

RUDN University

Cite This Article

Alexey A. Festa, Olga A. Storozhenko, Leonid G. Voskressensky, et al. (2023). Visible light-mediated halogenation of organic compounds. Chemical Society Reviews, 52(24), 8678-8698. https://doi.org/10.1039/d3cs00366c

Visible light-mediated halogenation of organic compounds

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