Oximes are valuable synthetic building blocks with reactivity modes that enable their use in
diverse methodologies, from cycloadditions to bioconjugation. Their reactivity towards …

A multifaceted study on the effect of various factors on the efficiency of photocyclization of
naphthofuran O‐acyl oximes was performed. It showed that without any additives or in the …

A detailed study of iminyl radical cyclizations of O-aryloximes tethered to alkenes is reported.
The reactions can be triggered by either microwave irradiation or conventional heating in an …

Pyrroline derivatives are common in bioactive natural products and therapeutic agents. We
report here a synthesis of pyrrolines and fused diaziridines by divergent radical cyclization of …

The fluorinated 5‐membered N‐containing heterocyclic compounds have wide utility in
varied fields. The importance of these compounds has encouraged researchers to explore …

The indolizidine core of virosinine A was synthesized by means of a microwave-promoted
cascade reaction featuring 5-exo-trig iminyl radical cyclization, thiyl radical elimination, and …

Described herein is a sequential thiolation reaction between tetrahydrocarbazol-4-one
oximes and aryl thiols, affording a wide range of 1, 3-dithiolated carbazol-4-amines, which …

Microwave irradiation of O-phenyloximes triggers N–O homolysis and 1, 5-hydrogen atom
transfer (HAT), resulting in formal γ-C–H functionalization of ketones after trapping of the …

Novel Furan-ring Fused Chalcones (FFC) were synthesized using a radical cyclization
reaction of α, β-unsaturated ketones with cyclic ketone as the model reaction to attain this …

A tandem one-pot strategy for the synthesis of 4-iodo-3-aryl (alkyl)-1H-pyrano [4, 3-b]
quinolin-1-ones and (E)-3-(iodo (phenyl) methylene) isobenzofuran-1-(3H)-ones from 2 …