Catalyst free, C-3 functionalization of imidazo[1,2-a]pyridines to rapidly access new chemical space for drug discovery efforts. [PDF]
Gunaganti N +6 more
europepmc +1 more source
HPW-Catalyzed environmentally benign approach to imidazo[1,2-a]pyridines. [PDF]
Martinho LA, Andrade CKZ.
europepmc +1 more source
Synthesis of 6- or 8-Carboxamido Derivatives of Imidazo[1,2-a]pyridines via a Heterogeneous Catalytic Aminocarbonylation Reaction. [PDF]
Nagy E +3 more
europepmc +1 more source
One-pot CuI/l-proline-catalysed multicomponent synthesis of pyrido[2',1':2,3]imidazo[4,5-<i>c</i>]quinoline derivatives from 2-(2-bromophenyl)imidazo[1,2-<i>a</i>]pyridines, NH<sub>3</sub> and DMSO under air. [PDF]
Phuc BV +9 more
europepmc +1 more source
Highly Enantioselective Lewis Acid Catalyzed Conjugate Addition of Imidazo[1,2-a]pyridines to α,β-Unsaturated 2-Acylimidazoles under Mild Conditions. [PDF]
C Thedy ME +8 more
europepmc +1 more source
One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction. [PDF]
Yang B, Tao C, Shao T, Gong J, Che C.
europepmc +1 more source
8-Aryl-6-chloro-3-nitro-2-(phenylsulfonylmethyl)imidazo[1,2-a]pyridines as potent antitrypanosomatid molecules bioactivated by type 1 nitroreductases. [PDF]
Fersing C +20 more
europepmc +1 more source
Substituted imidazo[1,2-a]pyridines as β-strand peptidomimetics. [PDF]
Kang CW, Sun Y, Del Valle JR.
europepmc +1 more source

