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[1]
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Synthetic Utility of the Vilsmeier–Haack Reagent in Organic Synthesis
Synlett,
2023
DOI:10.1055/s-0042-1751421
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[2]
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Trichloroisocyanuric acid (TCCA) and carboxamide interactions in TCCA/NaNO2 triggered nitration of pyrrole and indole in aqueous aprotic media: A kinetic correlation of solvent properties with reactivity
International Journal of Chemical Kinetics,
2021
DOI:10.1002/kin.21432
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[3]
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Trichloroisocyanuric acid (TCCA) and carboxamide interactions in TCCA/NaNO
2
triggered nitration of pyrrole and indole in aqueous aprotic media: A kinetic correlation of solvent properties with reactivity
International Journal of Chemical Kinetics,
2020
DOI:10.1002/kin.21432
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[4]
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A review on synthetic procedures and applications of phosphorus oxychloride (POCl3) in the last biennial period (2018–19)
Phosphorus, Sulfur, and Silicon and the Related Elements,
2020
DOI:10.1080/10426507.2020.1831499
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[5]
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Ultrasonically Assisted Decarboxylative Bromination of α,β-Unsaturated Carboxylic Acids Under Vilsmeier-Haack Conditions
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry,
2016
DOI:10.1080/15533174.2014.989573
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[6]
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Prussian Blue as an Eco-Friendly Catalyst for Selective Nitration of Organic Compounds Under Conventional and Nonconventional Conditions
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry,
2014
DOI:10.1080/15533174.2013.770759
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[7]
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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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[8]
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Selective Nitration of Phenolic Compounds by Green Synthetic Approaches
Synthetic Communications,
2014
DOI:10.1080/00397911.2014.896925
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[9]
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Environmentally benign contemporary Friedel–Crafts acylation of 1-halo-2-methoxynaphthalenes and its related compounds under conventional and nonconventional conditions
Tetrahedron Letters,
2013
DOI:10.1016/j.tetlet.2013.04.075
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[10]
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Efficient Catalytic Activity of Transition Metal Ions in Vilsmeier-Haack Reactions with Acetophenones
International Journal of Chemical Kinetics,
2013
DOI:10.1002/kin.20807
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[11]
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Oxalylchloride/DMF as an Efficient Reagent for Nitration of Aromatic Compounds and Nitro Decarboxylation of Cinnamic Acids in Presence of KNO3 or NaNO2 Under Conventional and Nonconventional Conditions
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry,
2013
DOI:10.1080/15533174.2012.752395
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[12]
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Efficient Catalytic Activity of Transition Metal Ions in Vilsmeier–Haack Reactions with Acetophenones
International Journal of Chemical Kinetics,
2013
DOI:10.1002/kin.20807
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[13]
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Aromatic nitration under neutral conditions using N-bromosuccinimide/silver(I) nitrate
Tetrahedron Letters,
2012
DOI:10.1016/j.tetlet.2012.06.126
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[14]
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Ultrasonically Assisted Synthesis of Aromatic Sulfonic Acids under Vilsmeier Haack Conditions in Acetonitrile Medium
International Journal of Organic Chemistry,
2012
DOI:10.4236/ijoc.2012.24046
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[15]
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Ultrasonically Assisted Regioselective Nitration of Aromatic Compounds in Presence of Certain Group V and VI Metal Salts
Green and Sustainable Chemistry,
2012
DOI:10.4236/gsc.2012.23015
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