We developed a sustainable three-component reductive amination protocol for the
chemoselective coupling of optically active functionally rich donor–acceptor carbonyl …

We developed a simple and practically feasible protocol for the chemoselective coupling of
optically active functionally rich 2-aroylcyclopropanecarbaldehydes with various CH acids or …

A simple two-step dialkylation protocol was developed to synthesize biologically active
antibiotics photopyrones, pseudopyronines, and violapyrones from bio-renewable triacetate …

Besides numerous synthetic and biological applications, the catalytic construction of chiral
Swaminathan ketones and their analogues possessing a bicyclo [5.4. 0] undecane core …

To date, a general approach for the direct α-acyloxylation of cyclic 1, 3-dicarbonyls remains
challenging. Herein, we report a Pd-catalyzed α-acyloxylation of cyclic 1, 3-dicarbonyl …

Readily available 3-alkylideneoxindoles were effectively reduced to 3-alkyloxindoles
through transfer hydrogenation using Hantzsch ester as a reducing agent at ambient …