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Synthesis of imidazo[1,2- a] pyridines directly from methyl or methylene ketones. iodination of imidazo[1,2-a] pyridines

Chemistry of Heterocyclic Compounds, 1976
Imidazo[1,2-a]pyridines were obtained by direct reaction of acetophenone, propiophenone, and their furan analogs and ring-substituted derivatives with an equimolar amount of iodine and and excess 2-aminopyridine or its substituted derivatives. The effect of substituents in the ketones and 2-aminopyridine, the reagent molar ratios, the character of the ...
N. O. Saldabol, S. A. Giller
openaire   +1 more source

Imidazo[1,2-a]pyridine Scaffold as Prospective Therapeutic Agents

Current Topics in Medicinal Chemistry, 2016
Imidazo[1,2-a]pyridine is one of the most potential bicyclic 5-6 heterocyclic rings that is recognized as a "drug prejudice" scaffold due to its broad range of applications in medicinal chemistry such as anticancer, antimycobacterial, antileishmanial, anticonvulsant, antimicrobial, antiviral, antidiabetic, proton pump inhibitor, insecticidal activities.
Aakash, Deep   +8 more
openaire   +2 more sources

ChemInform Abstract: Imidazo(1,2‐a)pyridines. Part 2. Ozonolysis of Imidazo(1,2‐a)pyridines and Synthesis of Cardiotonic Agents.

ChemInform, 1992
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
M. YAMANAKA   +3 more
openaire   +1 more source

Novel imidazo[2,1-b]thiazoles and imidazo[1,2-a]pyridines tethered with indolinone motif as VEGFR-2 inhibitors and apoptotic inducers: Design, synthesis and biological evaluations.

Bioorganic chemistry (Print)
The current study investigates the anticancer and VEGFR-2 inhibitory activities of 16 novel indolinone-grafted imidazo[2,1-b]thiazole and imidazo[1,2-a]pyridine derivatives (6a-h and 10a-h).
Mahmoud S. Elkotamy   +5 more
semanticscholar   +1 more source

Organotin(IV) complexes with imidazo[1,2-a]pyridines

Polyhedron, 2014
Abstract The three-components reaction of dimethyltin dibromide with imidazo[1,2-a]pyridine and allyl bromide in ethanol affords an ionic complex, bis(1-allylimidazo[1,2-a]pyridinium) dimethyltetrabromostannate(II). X-ray crystal structure analysis of the complex reveals the tin atom to be hexacoordinated, forming a dianion.
Rati Agrawal   +6 more
openaire   +1 more source

ChemInform Abstract: Photoisomerization of Imidazo(1,2‐a)pyridines.

ChemInform, 1997
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
R. KUBIK   +3 more
openaire   +1 more source

Discovery of imidazo[1,2-a]pyridines as potent MCH1R antagonists

Bioorganic & Medicinal Chemistry Letters, 2009
A series of imidazo[1,2-a]pyridine derivatives was identified and evaluated for MCH1R binding and antagonistic activity. Introduction of a methyl substituent at the 3-position of imidazo[1,2-a]pyridine provided compounds with a significant improvement in MCH1R affinity.
Hiroyuki, Kishino   +13 more
openaire   +2 more sources

Synthesis of Imidazo[1,2-a]pyridine Derivatives as Antiviral Agents

Arzneimittelforschung, 2011
The synthesis and antiviral activity of original dibromoimidazo[1,2-a]pyridines bearing a thioether side chain are reported. Molecular modeling was used to identify biophoric structural patterns that are common to 16 compounds. Structure-activity relationship (SAR) studies identified hydrophobicity (logP) as the most important factor for activity. From
S, Mavel   +7 more
openaire   +2 more sources

Reactions of 1‐Substituted Benz[4,5]imidazo[1,2‐a]pyridines.

ChemInform, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
Yu. M. Volovenko   +2 more
openaire   +1 more source

Visible-Light-Promoted and EDA Complex-Driven [4 + 2] Annulation for the Construction of Naphtho[1',2':4,5]imidazo[1,2-a]pyridines.

Organic Letters
A green visible-light-promoted and electron donor-acceptor (EDA) complex-driven synthetic strategy for the construction of value-added naphtho[1',2':4,5]imidazo[1,2-a]pyridines from 2-arylimidazo[1,2-a]pyridines with Z-α-bromocinnamaldehydes has been ...
Wanting Feng   +9 more
semanticscholar   +1 more source

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