In recent years, para-quinone methides (p-QMs) have emerged as attractive and versatile
synthons in organic synthesis owing to their high reactivity. Consequently, p-QM chemistry …

para‐Quinone methides (p‐QMs) are naturally occurring molecules that have been finding
increasing synthetic applications in the last few years. The presence of two electronically …

Over the years, quinone methides have broadly been applied in synthesis and biological
systems for synthesizing heterocyclic compounds and biologically active molecules. In this …

A metal and base‐free, operationally simple, and scalable multicomponent approach
towards the synthesis of S‐diarylmethane dithiocarbamates is reported. A range of …

A simple and powerful one-pot regioselective 1, 6-addition elimination–6π-aza-
electrocyclization–aromatization reaction of vinyl/dienyl-substituted para-quinone methides …

Azaheterocycles are one of the most prevalent classes of compounds present in numerous
bioactive compounds, natural products, and agrochemicals, and undoubtedly, new methods …

An expeditious, cost-effective synthetic methodology for a wide range of nitrogen-containing
unsymmetrical trisubstituted methanes (TRSMs) is reported. The synthesis involves base …

Abstract An efficient Zn (OTf) 2-catalyzed regioselective C–N bond making reaction between
a bunch of aryl/heteroaryl-substituted para-quinone methides as ideal 1, 6-acceptors and …

Reactions of para-quinone methides (p-QMs) with α-diazo-β-ketosulfones and their
corresponding esters as well as simple β-dicarbonyl compounds and β-ketosulfones have …

This review explores the significance of trifluoromethylnitrones in synthesizing fluorine-
containing compounds, with a particular focus on trifluoromethylated heterocycles. It …