Homogeneous gold catalysis has demonstrated the preponderant capability of realizing a
broad range of synthetically versatile alkyne functionalization over the last two decades …

Gold complexes, because of their unique carbophilic nature, have evolved as efficient
catalysts for catalyzing various functionalization reactions of C–C multiple bonds. However …

An efficient strategy for the one-pot synthesis of polysubstituted pyridines via a cascade
reaction from aldehydes, phosphorus ylides, and propargyl azide is reported. The reaction …

Total synthesis of (±)-taiwaniaquinol F (1a) has been accomplished via an efficient Lewis
acid-catalyzed Nazarov-type cyclization of aryldiallylcarbinols (±)-2e derived from safranal 7 …

The construction of complex polycyclic terpenoid products in an efficient and step‐
economical manner using multicomponent and tandem processes is highly valuable …

Cooperative catalysis is a powerful strategy to improve the efficiency and selectivity of
organic reactions. It is of current interest in asymmetric catalysis to combine different …

A novel method for the synthesis of fused pyrimido [1, 6-a]-indolone derivatives by
annulation of 2-alkynylaryl aldehydes/2-alkynylarylidene ketones with N-(pivaloyloxy)-1H …

A general approach to the synthesis of 1, 3-disubstituted-1, 2-dihydroisoquinolines was
achieved with pyrrole and various electron withdrawing groups as substituents. CuAAC …

FeCl3‐catalyzed cyclization of an arylvinyl carbinols has been explored for efficient
synthesis of [6, 5, 6]‐carbotricyclic core of taiwaniaquinoids sharing an all‐carbon …

The first organocatalytic asymmetric inverse‐electron‐demand Diels–Alder reaction of
deconjugated enones by using a linear dienamine was explored. Electron‐poor oxadienes …