Hydrofunctionalization of alkynes is one of the most efficient ways to access axially chiral
styrenes with open‐chained olefins. While great advances have been achieved for 1 …

A green, efficient and highly regioselective synthesis of flavonoids and their derivatives from
β-phenoxyl ynones using wet 1, 3-propanediol as reaction medium was developed, without …

An efficient reagent-free method for the synthesis of polysubstituted 4-quinolone from 2-
substituted alkynoyl aryl-sulfonamide was developed. This developed method tolerates …

The secondary metabolites from Hericium erinaceus are well-known to have neurotrophic
and neuroprotective effects. Isohericerinol A (1), isolated by our colleagues from its fruiting …

A catalyst-free, additive-free, and eco-friendly method for synthesizing 1, 2, 4-triazolo [1, 5-a]
pyridines under microwave conditions has been established. This tandem reaction involves …

A robust metal-and solvent-free cascade radical-induced CN cleavage/intramolecular 6-
endo-dig annulation/hydrocarbonylation for the synthesis of the valuable 2-aryl-4 H …

In this study, we developed a reliable and atomic efficient nongaseous carbonylation
protocol to synthesize flavones under mild reaction conditions. By using a controlled CO …

The organic ring closure reaction of diverse acyclic compounds is governed mostly by the
Baldwin rule. The ring closure compounds shows emergent application. In recent years, ring …

A 2D Dy (III) metal–organic layer (MOL 1) was synthesized under solvothermal conditions.
Structural analysis suggests that the Dy (III) ions in each one-dimensional (1D) arrangement …

The amine‐promoted rearrangement of 3‐halogenated and 3‐tosylated flavones into amino‐
substituted aurones is a reliable but little‐explored method in aurone synthesis. We extend it …