γ-Butyrolactone, a five-membered lactone moiety, is one of the privileged structures of
diverse natural products and biologically active small molecules. Because of their broad …

Terpenoids with lactone moieties have been indicated to possess high bioactivity. Certain
terpenoid lactones exist in nature, in plants and animals, but they can also be obtained by …

An I2-mediated metal-free oxidative C–N bond formation methodology has been established
for the regioselective pyrazole synthesis. This practical and eco-friendly one-pot protocol …

An operationally simple and high yielding protocol for the synthesis of polyfunctional
pyrazoles has been developed through one-pot, three-component coupling of aldehydes, 1 …

A general and unprecedented gold-catalyzed tandem dual heterocyclization reaction of
enynones with 1, 3, 5-triazines has been developed, which provides bicyclic fused furans in …

Novel enamine derivatives were synthesized from the reaction of lactone and chalcones and
their antiproliferative and cytotoxic activities against six cancer cell lines (eg, HeLa, HT29 …

The enantiomers of four chiral 3-aryl-substituted-γ-butyrolactones, key intermediates for the
preparation of compounds of pharmaceutical interest, were successfully isolated by …

This study focuses on understanding the structural and molecular changes in lipid
membranes under the influence of six halogenated flavonoid derivatives differing in the …

A sequential two‐step chemoenzymatic methodology for the stereoselective synthesis of
(3E)‐4‐(het) arylbut‐3‐en‐2‐amines in a highly selective manner and under mild reaction …

Herein, we report the synthesis of 3-carbonyl-trisubstituted furans via Pd-catalyzed oxidative
cycloisomerization reactions of 2-alkenyl-1, 3-dicarbonyl scaffolds, using molecular oxygen …