Periodic acid-promoted methylenation of imidazoheteroarenes: a green approach using ethylene glycol as a C1 source. [PDF]
Franco MS +6 more
europepmc +1 more source
Copper-catalyzed three-component reaction to synthesize polysubstituted imidazo[1,2-a]pyridines. [PDF]
Zhou Z +5 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
Synthetic Imidazopyridine-Based Derivatives as Potential Inhibitors against Multi-Drug Resistant Bacterial Infections: A Review. [PDF]
Sanapalli BKR +5 more
europepmc +1 more source
A copper bromide-decorated magnetic oyster shell biosupport as a sustainable catalyst for heterogeneous synthesis of imidazo[1,2-<i>a</i>]pyridines in glycerol. [PDF]
Ansari S +3 more
europepmc +1 more source
Iodine catalyzed synthesis of imidazo[1,2-a]pyrazine and imidazo[1,2-a]pyridine derivatives and their anticancer activity. [PDF]
Krishnamoorthy R, Anaikutti P.
europepmc +1 more source
Cu(II)-Catalyzed Synthesis of Benzo[4,5]Imidazo[2,1-b]Thiazole Using Nitroalkene and 1H-Benzo[D]Imidazole-2-Thiol [PDF]
Hajra, A., Jana, S.
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Synthetic approaches towards novel isoform selective pi3k inhibitors and their biological activities against prostate cancer cells, 2018 [PDF]
The development of novel imidazopyridines, which includes both tetrahydroimidazo[1,5-a]pyridine (rIMP) and imidazo[1,5-a]pyridine (IMP) was investigated using conventional and microwave induced procedures that afforded compounds at high yield of 88-96 ...
core +1 more source
Simple synthesis of 2-(phenylsulphinyl)benzo[d]oxazole derivatives via a silver-catalysed tandem condensation reaction. [PDF]
Xu R, Hu Q, Hu J, Liu G, Xu J.
europepmc +1 more source
Synthesis and evaluation of novel heterocyclic compounds as anticancer agents [PDF]
There is a clear need for anti-cancer therapies that have effective cytotoxic efficiency andmarginal toxicity, preferably zero. For this goal, researchers have been persevering todevelop new drugs from natural resources. Among them are agents that target
Mal ullah, AARA
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