<i>p</i>‑Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN₃ for Synthesis of 4‑Aryl-<i>NH</i>-1,2,3-triazoles

A p-TsOH-mediated 1,3-dipolar cycloaddition of nitroolefins and sodium azide for the synthesis of 4-aryl-NH-1,2,3-triazoles has been developed. p-TsOH was discovered as a vital additive in this type of 1,3-dipolar cycloaddition. This novel cycloaddition reaction is a good method for the rapid synthesis of valuable 4-aryl-NH-1,2,3-triazoles in high yields

Correction to <i>p</i>‑Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN₃ for Synthesis of 4‑Aryl-<i>NH</i>-1,2,3-triazoles

Correction to <i>p</i>‑Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN₃ for Synthesis of 4‑Aryl-<i>NH</i>-1,2,3-triazole

A Facile BPO-Mediated <i>ortho</i>-Hydroxylation and Benzoylation of <i>N</i>‑Alkyl Anilines for Synthesis of 2‑Benzamidophenols

A facile benzoyl peroxide (BPO) mediated <i>ortho</i>-hydroxylation and benzoylation of <i>N</i>-alkyl anilines for the synthesis of 2-benzamido­phenols has been developed. The reaction tolerates a wide range of functional groups and is a good method for the straightforward synthesis of valuable 2-benzamido­phenols in good yields under mild conditions