Sequential reactions of aminoalkynes represent a powerful tool to easily assembly
biologically important polyfunctionalized nitrogen heterocyclic scaffolds. Metal catalysis …

ABSTRACT A metal-free, atom-economy and simple work-up domino amination-
Knoevenagel condensation approach to construct new coumarin analogous (4a-f and 8a-e) …

An efficient Au (I)-catalyzed intramolecular cascade reaction of tertiary enamides tethered an
alkynyl group has been developed. The process is composed of a propargyl-claisen …

Herein, we synthesized biological magnetic glycoluril tetrakis (methylene phosphorous acid)
as a new heterogeneous nano-catalyst. The magnetic nano-catalyst Fe3O4@ GTMPA was …

A Cu-catalyzed, easily scalable one-pot synthesis of fused pyridines by the reaction of cyclic
ketones with propargylamine is described. The protocol was optimized based on the results …

An iodoxybenzoic acid-mediated selected oxidative cyclization of N-hydroxyalkyl enamines
was developed. Through this strategy, a variety of 2, 3-disubstituted pyrroles and pyridines …

Pericyclic reactions present a convenient tool for constructing heterocyclic systems. They
make possible to obtain quite complex structures in one step with high yields and …

β-Amino-α, β-enones or β-enamino carbonyl compounds are versatile synthons
intermediates for the construction of various bio-active heterocyclic compounds and have …

An efficient tandem reaction of β-enaminoesters and 1, 3-diarylpropenes is disclosed. It
undergoes oxidative coupling mediated by DDQ, subsequent intermolecular cyclization and …

We describe a one-pot strategy to access 3-carboxyl-and 3-ketopyridines from readily
available alkynes and propargylamine via a hydroamination process. This one-pot protocol …