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 …

In the last few years, there has been an explosive growth in the area of para‐quinone
methide (p‐QM) chemistry. This boom is actually due to the unique reactivity pattern of p …

An unprecedented umpolung spirocyclopropanation reaction of p-quinone methides and α-
keto carbonyls is described. Our umpolung strategy based on 1, 6-conjugate addition and …

A base-promoted olefin skeletal rearrangement strategy from para-quinone methides (p-
QMs) and N-fluoroarenesulfonamides is reported, enabling direct nitrogen insertion of …

An unprecedented approach to synthesize spirobutyrolactone para-dienones from para-
quinone methides and bromo-Meldrum's acids has been developed. A series of spatially …

A catalyst-free and controllable reaction of isatin-derived para-quinone methides with sulfur
ylides was developed. This protocol enables the divergent synthesis of two different …

The stereoselective sequential spirocyclopropanation/Cloke–Wilson rearrangement
reactions have been developed to synthesize γ-butyrolactones using alkylidene Meldrum's …

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

A two-step formal (4+ 1) annulation-dehydration reaction offers a convenient route to C2-
arylated indoles and benzofurans. This reaction exploits the bifunctional reactivity of electron …