نتایج جستجو برای: substituted imidazoles

تعداد نتایج: 42509  

Journal: :Molecules 2009
Yuka Kawashita Masahiko Hayashi

A variety of heteroaromatic compounds, such as substituted pyridines, pyrazoles, indoles, 2-substituted imidazoles, 2-substituted imidazoles, 2-arylbenzazoles and pyrimidin-2(1H)-ones are synthesized by oxidative aromatization using the activated carbon and molecular oxygen system. Mechanistic study focused on the role of activated carbon in the synthesis of 2-arylbenzazoles is also discussed. ...

2014
Debasish Bandyopadhyay Lauren C Smith Daniel R Garcia Ram N Yadav Bimal K Banik

BACKGROUND Azaheterocycles are an important class of compounds because of their highly potent medicinal activities, and the imidazole subcategory is of special interest in regard to drug discovery research. FINDINGS An expeditious synthetic protocol of 2-aryl-4-phenyl-1H-imidazoles has been accomplished by reacting phenylglyoxal monohydrate, ammonium acetate, and aldehyde under sonication. Fo...

2009
Ajay Kumar Dubey Neeraj Kumar Manmohan Singh Anil Pratap Singh Praveen Kumar Ashok

Di & tri substituted imidazoles were prepared by condensing phenylglyoxal with different aryl aldehydes in presence of ammonium acetate and glacial acetic acid. All the di and tri substituted imidazoles were characterized by spectral analysis i.e. HNMR and Mass spectral data. All the synthetic compounds were screened for there anti-inflammatory and anti bacterial activity.

Journal: :Chemical communications 2014
Thibaut Alzieu Johannes Lehmann Ajay B Naidu Rainer E Martin Robert Britton

We report the optimization of a neglected reaction for the rapid and direct conversion of oxazoles into N-substituted imidazoles. The utility of this microwave-promoted reaction for diversity-oriented synthesis is demonstrated in the preparation of >40 N-substituted imidazoles, including α-imidazolyl esters.

Journal: :Journal of Synthetic Organic Chemistry, Japan 1998

Journal: :organic chemistry research 2016
seyyed jafar saghanezhad alireza kiasat

one-pot preparation of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles has been conducted in the presence of poly(4-vinylpyridinium butane sulfonic acid) hydrogen sulfate, p(4vpbsa)hso4, as an efficient dual acidic catalyst under solvent-free conditions. reusability of the catalyst, easy work-up procedure, eco-friendly reaction conditions, short reaction times and high yields of th...

Journal: :Chemical communications 2011
Juventino J García Paulina Zerecero-Silva Grisell Reyes-Rios Marco G Crestani Alma Arévalo Rigoberto Barrios-Francisco

Nickel(0) catalysts were used to produce substituted imidazoles in good to high yields using benzonitrile, p-substituted benzonitriles and 4-cyanopyridine as starting materials.

2011
Baskar Lakshmanan Papiya Mitra Mazumder D. Sasmal Simon Santosh Jena

Anthelmintic resistance creates a major hitch over the decades throughout the world. As per WHO only few drugs are frequently used in the treatment of helminth infestations in human beings. In view of this, an attempt has been made to study the anthelmintic activity of some newly synthesized 1-substituted imidazoles (1a-1d, 2a-2d) were synthesized and characterized by their spectral data. All t...

Journal: :Green and Sustainable Chemistry 2023

Substituted imidazoles are of interest because their useful biological activities. While several methods have been developed for the synthesis such compounds, some reported utilize corrosive or toxic catalysts. We report a bismuth (III) triflate catalyzed multicomponent 2,4,5-trisubstituted imidazoles. Bismuth compounds attractive from green chemistry perspective they remarkably non-toxic and n...

Journal: :Organic letters 2004
Scott E Wolkenberg David D Wisnoski William H Leister Yi Wang Zhijian Zhao Craig W Lindsley

[reaction: see text] A simple, high-yielding synthesis of 2,4,5-trisubstituted imidazoles from 1,2-diketones and aldehydes in the presence of NH(4)OAc is described. Under microwave irradiation, alkyl-, aryl-, and heteroaryl-substituted imidazoles are formed in yields ranging from 80 to 99%. Short syntheses of lepidiline B and trifenagrel illustrate the utility of this approach.

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