نتایج جستجو برای: N-Acylhydrazones

تعداد نتایج: 976508  

2016
Mauro Carcelli Dominga Rogolino Anna Gatti Laura De Luca Mario Sechi Gyanendra Kumar Stephen W. White Annelies Stevaert Lieve Naesens

Influenza virus PA endonuclease has recently emerged as an attractive target for the development of novel antiviral therapeutics. This is an enzyme with divalent metal ion(s) (Mg(2+) or Mn(2+)) in its catalytic site: chelation of these metal cofactors is an attractive strategy to inhibit enzymatic activity. Here we report the activity of a series of N-acylhydrazones in an enzymatic assay with P...

Journal: :Dalton transactions 2014
Zhiyou Li Lamei Wu Tao Zhang Zhengxi Huang Guofu Qiu Zhongqiang Zhou Longfei Jin

N-Methyl-N'-2-hydroxybenzaldehyde acylhydrazones have been chemospecifically synthesized in good yield by N-methylation of the Fe(iii) complexes of N-2-hydroxybenzaldehyde acylhydrazones with methyl iodide in tetrahydrofuran. The reaction proceeds with the exclusive formation of the N-methyl derivative without any concurrent O-methylation side reactions. In addition, the N-methylation reaction ...

Journal: :Organic letters 2011
Jinshui Chen Burjor Captain Norito Takenaka

A highly enantioselective synthesis of homopropargylic alcohols is achieved by using the new helical chiral 2,2'-bipyridine N-monoxide catalyst and allenyltrichlorosilane. This method can be further extended to the enantio- and regioselective propargylation of N-acylhydrazones.

Journal: :Molecules 2015
Tiago Fernandes da Silva Walfrido Bispo Júnior Magna Suzana Alexandre-Moreira Fanny Nascimento Costa Carlos Eduardo da Silva Monteiro Fabio Furlan Ferreira Regina Cely Rodrigues Barroso François Noël Roberto Takashi Sudo Gisele Zapata-Sudo Lídia Moreira Lima Eliezer J Barreiro

The N-acylhydrazone (NAH) moiety is considered a privileged structure, being present in many compounds with diverse pharmacological activities. Among the activities attributed to NAH derivatives anti-inflammatory and analgesic ones are recurrent. As part of a research program aiming at the design of new analgesic and anti-inflammatory lead-candidates, a series of cyclohexyl-N-acylhydrazones 10-...

Journal: :Organic & biomolecular chemistry 2009
Ai-Fang Li Hui He Yi-Bin Ruan Zhen-Chang Wen Jin-Song Zhao Qiu-Ju Jiang Yun-Bao Jiang

A series of N-acylhydrazones were synthesised and found to be "turn-on" fluorescent chemodosimeters for Cu(2+). Among the tested transition metal ions such as Cu(2+), Pb(2+), Zn(2+), Cd(2+), Hg(2+), and Ni(2+), a prominent fluorescence enhancement of up to 1000-fold was only observed for Cu(2+) in acetonitrile (CH(3)CN). This was indicated by an onset of unprecedented structured emission. Detai...

Journal: :Molecules 2012
Cledualdo Soares de Oliveira Bruno Freitas Lira Vivyanne dos Santos Falcão-Silva Jose Pinto Siqueira Jose Maria Barbosa-Filho Petronio Filgueiras de Athayde-Filho

Five new 1-(2-(5-nitrofuran-2-yl)-5-(aryl)-1,3,4-oxadiazol-3-(2H)-yl) ethanone compounds 5a-e were synthesized by cyclization of N-acylhydrazones 4a-e with acetic anhydride under reflux conditions. Their structures were fully characterized by IR, ¹H-NMR, and ¹³C-NMR. Furthermore, evaluations of the antibacterial activity of the 1,3,4-oxadiazoles 5a-e and N-acylhydrazones 4a-e showed strong acti...

Journal: :Organic & biomolecular chemistry 2011
Gregory K Friestad An Ji Chandra Sekhar Korapala Jun Qin

Stereocontrolled Mn-mediated radical addition of alkyl iodides to chiral N-acylhydrazones enables strategic C-C bond disconnection of chiral amines. This strategy was examined in the context of a total synthesis of quinine, generating new findings of functional group compatibility leading to a revised strategy. Completion of a formal synthesis of quinine is presented, validating the application...

Journal: :Chemical communications 2009
Markus Albrecht Yufeng Liu Sascha S Zhu Christoph A Schalley Roland Fröhlich

Acylhydrazones of 2,3-dihydroxybenzaldehyde are easily accessible and afford heterodinuclear helicates; the self-assembly is specific when the resulting coordination compounds are neutral in charge.

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