Nitroxides, also known as nitroxyl radicals, are long-lived or stable radicals with the general
structure R1R2N–O•. The spin distribution over the nitroxide N and O atoms contributes to …

Recent advances in synthetic methodologies for selective, oxidative transformations using
Bobbitt's salt (4-acetamido-2, 2, 6, 6-tetramethyl-1-oxopiperidinium tetrafluoroborate, 1) and …

A range of acyl azoles have been prepared from aromatic, heteroaromatic, and aliphatic
aldehydes by means of an oxidative amidation reaction. The methodology employs a …

A protocol for the oxidation of alcohols to aldehydes and ketones employing an
electrochemical aminoxyl-mediated reaction is presented. The approach employs a catalytic …

CoSe was developed as an efficient electrocatalyst for ammoxidation of furfural (1a) and
aqueous ammonia to 2-furonitrile (3a) with in-situ formed furfurylimine (2a) as an …

Nitriles are employed in many academic and industrial fields, especially organic synthesis.
They are crucial precursors to synthesize aldehydes, amines, amides, carboxylic acids, and …

A methodology for the oxidation of α-trifluoromethyl alcohols to the corresponding
trifluoromethyl ketones is presented. A catalytic quantity of a nitroxide is used, and …

Background: Oxidation is a valuable tool in preparative organic chemistry. Oxoammonium
salts and nitroxides have proven valuable as reagents and catalysts in this endeavor …

Bis(1,1,1,3,3,3-hexafluoropropan-2-yl) [1,1′-biphenyl]-4,4′-dicarboxylate
Previous Article in Journal 6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one search …