Results 71 to 80 of about 81,920,088 (159)

Copper-catalyzed three-component reaction to synthesize polysubstituted imidazo[1,2-a]pyridines. [PDF]

RSC Adv, 2022
Zhou Z, Luo D, Li G, Yang Z, Cui L, Yang W.   +5 more
europepmc   +1 more source

Development of Dimethylisoxazole-Attached Imidazo[1,2-a]pyridines as Potent and Selective CBP/P300 Inhibitors. [PDF]

J Med Chem, 2021
Muthengi A, Wimalasena VK, Yosief HO, Bikowitz MJ, Sigua LH, Wang T, Li D, Gaieb Z, Dhawan G, Liu S, Erickson J, Amaro RE, Schönbrunn E, Qi J, Zhang W.   +14 more
europepmc   +1 more source

Cu(OTf)₂-catalyzed synthesis of imidazo[1,2-a]pyridines from α-diazoketones and 2-aminopyridines

, 2007
α-Diazoketones undergo smooth coupling with 2-aminopyridines in the presence of 10 mol % of copper(II) triflate to produce the corresponding 2-substituted imidazo[1,2-a]pyridines (IPs) in excellent yields with high selectivity.
Narsaiah, A. V., Gopal Rao, Y., Srinivas, M., Yadav, J. S., Subba Reddy, B. V.   +4 more
core   +1 more source

Molecular Iodine-Catalyzed Synthesis of Imidazo[1,2-a]Pyridines: Screening of Their In Silico Selectivity, Binding Affinity to Biological Targets, and Density Functional Theory Studies Insight. [PDF]

ACS Omega, 2022
Geedkar D, Kumar A, Sharma P.
europepmc   +1 more source

Synthesis of 2-(5-Nitropyrid-2-yl)-3-(4-substitutedphenyl)aminoisoxazol-5(2H)-ones and Their Rearrangements to Imidazo[1,2-a]- pyridines and Indoles with Triethylamine

, 2002
3-(4-Substitutedphenyl)aminoisoxazol-5(2H)-ones, substituted on nitrogen with a nitropyridine group, react with triethylamine to give imidazo[1,2-a]pyridines and indoles.
J. Khalafy, K. Akbari Dilmaghani, D. Setamdideh, K. Dilmaghani, K. Akbari Dilmaghani   +4 more
core   +1 more source

Hypervalent Iodine-Mediated Reaction of Anilines with Pyridines to Benzo[4,5]imidazo[1,2-a]pyridine Derivatives

, 2017
It was found that hypervalent iodine, such as (diacetoxyiodo)benzene and [bis(trifluoroacetoxy)iodo]benzene could mediate reaction of anilines with pyridines in mild reaction to give benzo[4,5]imidazo[1,2-a]pyridine derivatives.
Chen, Wun-Yu
core  

Novel Dicationic Imidazo[1,2-a]pyridines and 5,6,7,8-Tetrahydro-imidazo[1,2-a]pyridines as Antiprotozoal Agents

, 2016
2-[5-(4-Amidinophenyl)-furan-2-yl]-5,6,7,8-tetrahydro-imidazo[1,2-a]pyridine-6-carboxamidine acetate salt (7) was synthesized from 2-[5-(4-cyanophenyl)-furan-2-yl]-imidazo[1,2-a]pyridine-6-carbonitrile (4a), through the bis-O-acetoxyamidoxime followed by
Farial A. Tanious (2329273), W. David Wilson (7328), Tanja Wenzler (320253), David W. Boykin (148406), Reto Brun (41511), Mohamed A. Ismail (418629)   +5 more
core   +1 more source

Imidazo[1,2‑<i>a</i>]pyridines in Medicinal Chemistry: Recent Advances in Synthesis and Biological Activities. [PDF]

ACS Omega
Ferreira LAP, Caruso L, Nadur NF, Franco DP, Sousa GLS, Lacerda RB, Kümmerle AE.   +6 more
europepmc   +1 more source

Progress in the Field of Aldehyde Dehydrogenase Inhibitors: Novel Imidazo[1,2-a]pyridines against the 1A Family. [PDF]

ACS Med Chem Lett, 2020
Quattrini L, Gelardi ELM, Petrarolo G, Colombo G, Ferraris DM, Picarazzi F, Rizzi M, Garavaglia S, La Motta C.   +8 more
europepmc   +1 more source

I₂ and the Deep Eutectic Solvent ChCl-Tartaric Acid Promote the Addition-Oxidative Cyclization of 2-Aminopyridines and Chalcones to Obtain Imidazo[1,2-<i>a</i>]pyridines. [PDF]

Molecules
Lopez de Leon J, Cruces Velazco NM, Richaud A, Méndez F, Alonso DA, Contreras-Celedón CA.   +5 more
europepmc   +1 more source