Amine oxidation is one of the fundamental reactions in organic synthesis as it leads to a
variety of value‐added products such as oximes, nitriles, imines, and amides among many …

A metal-free system has been discovered for the efficient α-oxygenation of tertiary amines to
the corresponding amides using oxygen as an oxidant. This visible-light-mediated …

We present a convenient and efficient protocol to synthesize quinolines and quinazolines in
one pot under mild conditions. A variety of substituted quinolines were synthesized in good …

This protocol describes the use of 9-fluorenone as a cheap and non-toxic photocatalyst for
the oxidation of non-activated alcohols performed under the irradiation of a blue light …

A simple catalyst-and promoter-free protocol has been developed for the transamidation of
weakly nucleophilic aromatic amines with formamide derivatives and low-reactivity tertiary …

Ball milling of aromatic, heteroaromatic, vinylic, and aliphatic esters with ethanol and
calcium nitride afforded the corresponding primary amides in a transformation that was …

The highly desirable synthesis of the widely-used primary amides directly from alcohols and
ammonia via acceptorless dehydrogenative coupling represents a clean, atom-economical …

Base-metal catalysts Co1, Co2 and Co3 were synthesized from designed pincer ligands L1,
L2 and L3 having NNN donor atoms respectively. Co1, Co2 and Co3 were characterized by …

The dehydrogenation of amines has been identified as an efficient method for nitrile
synthesis. At present, this approach is restricted to (oxidative) dehydrogenations of primary …

Azido radical mediated photocatalytic oxidation method for the selective oxidation of various
well‐known feedstocks, such as (hetero) aromatic or aliphatic alcohols, alkylarenes, and …