A versatile Lewis acid catalyzed tandem cyclization of in situ generated alkynyl o-quinone
methides (o-AQMs) with electron-rich phenols has been developed on the basis of the mode …

A protocol involving intramolecular formal [4+ 2]‐cycloaddition of in situ generated o‐aza‐
quinone methide for the facile synthesis of 1, 4‐heterocycle‐fused quinoline motifs is …

A gold-catalyzed 6-endo-dig azide-yne cyclization/O–H insertion cascade reaction of azide-
tethered alkynes with alcohols has been developed, and it provides an expeditious access …

A new C-center radical-triggered bicyclization cascade of N-tethered 1, 7-enynes for forming
28 examples of biologically interesting spirocyclohexadienone-containing cyclopenta [c] …

An efficient [4+ 3] annulation of 2-(1-tosylalkyl) phenols with C, N-cyclic azomethine imines
via in situ generation of ortho-quinone methides (o-QMs) under mild basic reaction …

New synthetic approaches for the synthesis of indoloquinolines and carbocycle-fused
quinolines have been developed employing alkynylketone substrates. These synthetic …

A base-promoted (4+ 2) cyclization of aza-o-quinone methides (aza-o-QMs) in situ
generated from N-(o-chloromethyl) aryl amides was established. In this approach …

Selective C–H activation of a molecule containing multiple directing groups is an important
but challenging issue in organic chemistry. Herein, a combined directing group (hydrazone …

A novel tandem intermolecular ammonium ylide formation/intramolecular Mannich-type [5+
1] cyclization reaction of aryl diazoacetates and ortho-aminophenyl imine derivatives was …

We present a novel green synthetic protocol for the construction of a broad range of
substituted fused azabicyclo [3.3. 1] nonadiquinoline scaffolds through a formic acid …