has been cited by the following article(s):
[1]
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N‐Iodo‐4‐N,N‐Dimethylaminopyridinium Iodide; A New Green Iodination Reagent for Regioselective Mono and Di Iodination of Phenols and Anilines in Water with Good E‐Factor
ChemistrySelect,
2023
DOI:10.1002/slct.202204338
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[2]
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N‐Iodo‐4‐N,N‐Dimethylaminopyridinium Iodide; A New Green Iodination Reagent for Regioselective Mono and Di Iodination of Phenols and Anilines in Water with Good E‐Factor
ChemistrySelect,
2023
DOI:10.1002/slct.202204338
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[3]
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Bromide Oxidation: A Safe Strategy for Electrophilic Brominations
European Journal of Organic Chemistry,
2022
DOI:10.1002/ejoc.202200310
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[4]
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Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides
The Journal of Organic Chemistry,
2021
DOI:10.1021/acs.joc.1c00573
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[5]
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Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides
The Journal of Organic Chemistry,
2021
DOI:10.1021/acs.joc.1c00573
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[6]
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Recent Update on Transition Metal‐Free C(sp
2
)−H Bond Halogenation in (Hetero) Arenes
ChemistrySelect,
2021
DOI:10.1002/slct.202102956
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[7]
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Ultrasound-Assisted Bromination of Aromatic Rings Using NaBr/H2
O2
System
ChemistrySelect,
2017
DOI:10.1002/slct.201702023
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[8]
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Vanadium Pentoxide as a Catalyst for Regioselective Nitration of Organic Compounds under Conventional and Nonconventional Conditions
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry,
2014
DOI:10.1080/15533174.2013.790431
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