We report a versatile and functional-group-tolerant method for the Pd-catalyzed C–N cross-
coupling of five-membered heteroaryl halides with primary and secondary amines, an …

Two types of thiazole derivatives are synthesized through a multistep cascade sequence
with Pd-metalated phosphorus-doped porous organic polymers (POPs) as heterogeneous …

The asymmetric C–H bond functionalization reaction is one of the most efficient and
straightforward methods for the synthesis of optically active molecules. Herein, our work …

A series of fluorophores based on a thiazole core have been synthesized and shown to be
very sensitive to both structural changes and the microenvironment. Simple modifications of …

Xantphos is one of the two most common ligands used in palladium catalyzed Buchwald–
Hartwig amination reactions, because of its broad scope and high probability of success. It …

N, N‐diarylaminothiazoles containing cyano and nitro groups were synthesized using the Pd‐
catalyzed Buchwald‐Hartwig amination reaction with good yields. The cyano group in the …

Abstract A decarbonylative C− H coupling of azoles and aromatic esters by palladium
catalysis is described. Our previously reported Ni‐catalyzed C− H coupling of azoles and …

This work describes a new approach to construct highly conjugated molecules with
asymmetric donor‐acceptor‐donor'architectures (D− A− D'). Five new emissive compounds …

New fluorescent thiazoles were designed and synthesized based on a 3-aryl-2-(thiazol-2-yl)
acrylonitrile core. Three synthetic approaches were developed to introduce specific …

High functional group compatibility of iridium-catalyzed synthesis of enamines from amides
and 1, 1, 3, 3-tetramethyldisiloxane (TMDS) realized facile access of a series of donor (D)− π …