نتایج جستجو برای: multicomponent condensation

تعداد نتایج: 42157  

Journal: :ACS combinatorial science 2016
Isaivani Dhinakaran Vediappen Padmini Nattamai Bhuvanesh

A highly efficient, chemoselective synthesis of a library of polysubstituted pyrroles and tetrahydropyridines has been achieved through the one-pot, multicomponent reactions of ethyl (E)-3-(aryl/alkyl amino) acrylates, 2,2-dihydroxy-1-arylethan-1-ones, and malononitrile under solvent- and catalyst-free grinding conditions. The selective formation of pyrrole or tetrahydropyridines relied on subs...

2002
D. Lowe A. R. MacKenzie N. Nikiforakis

We present a condensed-mass advection based model (MADVEC) designed to simulate the condensation/evaporation of liquid polar stratospheric cloud (PSC) particles. A (Eulerian-in-radius) discretization scheme is used, making the model suitable for use in global or mesoscale chemistry and transport models (CTMs). The mass advection equations are solved using an adaption of the weighted average flu...

Journal: :Molbank 2022

We elaborated a convenient one-step approach for the synthesis of previously unknown 2-(5-acetyl-7-methoxy-2-(4-methoxyphenyl)benzofuran-3-yl)acetic acid. The suggested protocol includes multicomponent reaction acetovanillone, 4-methoxyphenylglyoxal and Meldrum’s have demonstrated that considered is one-pot telescoped process including preliminary condensation components in MeCN followed by aci...

An atom-efficient, eco-friendly, solvent-free, high yielding, multicomponent green strategy to synthesize triazolo[1,2-a]indazole-triones derivatives by the one-pot condensation of aldehyde, dimedone, and phenyl urazole is presented. A series of different substituted aromatic aldehydes including either electron-withdrawing or electron-donating groups used in this reaction participated well and ...

An atom-efficient, eco-friendly, solvent-free, high yielding, multicomponent green strategy to synthesize triazolo[1,2-a]indazole-triones derivatives by the one-pot condensation of aldehyde, dimedone, and phenyl urazole is presented. A series of different substituted aromatic aldehydes including either electron-withdrawing or electron-donating groups used in this reaction participated well and ...

Journal: :Organic & biomolecular chemistry 2009
Huanfeng Jiang Ronghuan Mai Hua Cao Qiuhua Zhu Xiaohang Liu

Highly functionalized multisubstituted 1,4-dihydropyridines 5 have been concisely synthesized in moderate to good yields via L-proline-catalyzed one-pot multicomponent reactions (MCRs) of alkynoates or alkynones 1, amines 2, beta-dicarbonyl compounds 3 and aldehydes 4 under mild conditions. The MCR process involves hydroamination/Knoevenagel condensation/Michael-type addition/intramolecular cyc...

Journal: :Molecules 2015
Yun-Peng Sui Hai-Ru Huo Jia-Jia Xin Jing Li Xiao-Jun Li Xin-Liang Du Hai Ma Hai-Yu Zhou Hong-Dan Zhan Zhu-Ju Wang Chun Li Feng Sui Ming-Kai Li

A novel series of biscoumarin (1-4) and dihydropyran (5-13) derivatives were synthesized via a one-pot multicomponent condensation reaction and evaluated for antibacterial and antitumor activity in vitro. The X-ray crystal structure analysis of four representative compounds, 3, 7, 9 and 11, confirmed the structures of these compounds. Compounds 1-4 showed the most potent antitumor activity amon...

Journal: :iranian journal of catalysis 2016
bijan mombeni goodajdar soghra soleimani

an atom-efficient, eco-friendly, solvent-free, high yielding, multicomponent green strategy to synthesize triazolo[1,2-a]indazole-triones derivatives by the one-pot condensation of aldehyde, dimedone, and phenyl urazole is presented. a series of different substituted aromatic aldehydes including either electron-withdrawing or electron-donating groups used in this reaction participated well and ...

Atefeh Nejatinejhad-Arani Morteza Shiri, Neil A. Koorbanally Suhas A. Shintre Zeynab Faghihi

Vilsmeier Several diamide derivatives containing 2-chloroquinoline scaffolds were synthesized via Ugi reaction of 2-chloroquinoline-3-carboxaldehydes, amines, carboxylic acids and isocyanides. The diversity of these quinolinyl Ugi-adducts was increased by using 2-chloroquinoline-3-carboxylic acids as a source of acid. Among them, compounds 2d, 2n, 2p, 4a, 4c and<strong...

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