This review describes the efforts in the synthesis of pyrrole derivatives using the reaction of
alkynes with nitrogen‐compounds under transition metal‐catalyzed and metal‐free …

Pyrrole is a versatile heterocyclic moiety exhibiting a wide range of pharmacological actions
with high therapeutic value. The importance of pyrrole in the pharmaceutical field lies in its …

The donor–acceptor system 4 having pyrazine scaffold as an acceptor moiety coupled to
donor amino groups through rotatable phenyl rings has been synthesized, which formed …

A straightforward method for the synthesis of functionalized imidazo [2, 1-b] thiazoles starting
from benzaldehydes, 2-aminothiazoles, and alkynes under copper (I, II) catalysis was …

Ruthenium(II)-Catalyzed Alkene C–H Bond Functionalization on Cinnamic Acids: A Facile
Synthesis of Versatile α-Pyrones | Organic Letters ACS ACS Publications C&EN CAS Find my …

A new carbon–carbon bond cleavage reaction was developed for the efficient synthesis of
multisubstituted pyrazolo [1, 5-a] pyrimidines. This base induced reaction of 1, 3, 5 …

Two new water-soluble phosphatriazene ligands have been synthesized as versatile
ligands for complexation reactions with Pd (OAc) 2 and utilized for catalyzing column-free …

With an aim to achieve a balance between ground-state and excited-state reduction
potential of donor acceptor systems for efficient C–N/C–C cross-coupling, a series of donor …

Pyrroles are the most prevalent heterocyclic compounds, which are present as the basic
cores in many natural products, such as vitamin B12, bile pigments like bilirubin and …

A one‐pot reaction of homopropargylic amines and aryl iodides was developed in the
presence of a palladium (Pd) catalyst and generated a series of tetrasubstituted pyrrole …