A methodology
is reported for preparing amides using amines as
an acyl source. The protocol involves the visible-light-promoted oxidative
amidation of amines with pyrazole to synthesize N-acyl pyrazoles followed by transamidation. By combining photoredox
catalysis with oxoammonium cations in the presence of sodium persulfate
as a terminal oxidant, the N-acyl pyrazoles could
be prepared efficiently and effectively using blue LEDs. The transamidation
step was performed without the need to purify the N-acyl pyrazole intermediate, and a range of amides were generated
in good to excellent yields.
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 substoichiometric quantity of an oxoammonium...
A simple, metal-free route for the oxidative esterification of aldehydes to yield hexafluoroisopropyl esters is reported. The methodology employs sodium persulfate and a catalytic quantity of a nitroxide and is...
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