نتایج جستجو برای: arylidene thio barbituric acids

تعداد نتایج: 269441  

Journal: :Molecules 2004
Nurettin Sadikov Sahin Nasibov Cemil Oğretir Halil Berber Ali Hüseyinli

The alkylation of beta-dicarbonyl compounds in a K2CO3/DMSO system was found to afford O- and C-alkylated derivatives, depending on the type of the beta-dicarbonyl compound involved. The alkyl derivatives obtained were used in the synthesis of some new spiro barbituric acid derivatives. Quantum chemical calculations were carried out to elucidate the reaction mechanisms for some typical synthesis.

Journal: :Chemical communications 2015
I A Karpenko A S Klymchenko S Gioria R Kreder I Shulov P Villa Y Mély M Hibert D Bonnet

Herein, we show that a far-red arylidene-squaraine dye is stable against nucleophiles, in contrast to arene-squaraines. Owing to the fluorescence enhancement in apolar media together with high brightness and photostability, this dye was successfully applied to detect the oxytocin G protein-coupled receptor and monitor its internalization in living cells.

Journal: :Organic & biomolecular chemistry 2012
Madhubabu Tatina Syed Khalid Yousuf Debaraj Mukherjee

Orthogonally protected monosaccharide building blocks have been prepared using TCT in a one-pot multicomponent transformation. The process involves successive steps of arylidene acetalation, esterification and regioselective reductive acetal cleavage. High regioselectivity, scope for using a broad range of substrates, functional group tolerance, mild reaction conditions, easy handling process a...

Journal: :Molecules 2007
Zuhal Turgut Cigdem Yolacan Feray Aydogan Emine Bagdatli Nuket Ocal

The synthesis of new 2,3,5,6-aryl substituted tetrahydro-2H-pyrazolo[3,4-d]- thiazoles 4a-j as potential biologically active compounds by the cyclocondensation of phenyl hydrazine with new 5-arylidene derivatives 2a-j of 2,3-disubstituted-1,3- thiazolidin-4-ones 1a-e is reported.

2012
Gheorghe-Doru Roiban Tatiana Soler Maria Contel Ion Grosu Carlos Cativiela Esteban P. Urriolabeitia

An efficient and high-yield procedure to prepare methyl N-benzoylamino-3-arylacrylates from unsaturated (Z)-2-aryl-4-arylidene-5-(4H)-oxazolones and Hg(OAc)2 in methanol is described herein. The observed reactivity of mercury(II) acetate here is different to its usual metallating behaviour, since it cleaves the unsaturated oxazolone ring without change of stereochemistry.

Journal: :The Journal of organic chemistry 2005
Yong-Gui Zhou Peng-Yu Yang Xiu-Wen Han

Highly enantioselective hydrogenation of exocyclic enamides, (Z)-3-arylidene-4-acyl-3,4-dihydro-2H-benzoxazines, was achieved in up to 98.6% ee by using Rh/(R,R)-Me-Duphos complex as the catalytic system. The absolute configuration of the product was assigned as R by chemical interrelations.

Journal: :Journal of mass spectrometry : JMS 2006
Eduardo C Meurer Marcos N Eberlin

We have already shown that the in-vacuum gas-phase Meerwein reaction of (thio)acylium ions is general in nature and useful for class-selective screening of cyclic (thio)epoxides. Herein we report that this gas-phase reaction can also be performed efficiently at atmospheric pressure under both electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) conditions. This alte...

Journal: :Chemistry 2022

β-carboline consists of a pyridine ring fused to an indole skeleton; it possesses numerous pharmacological activities, including anticancer. Previously, we reported satisfactory 2D and 3D QSAR study on derivatives. Based studies, designed, synthesized, characterized, screened fourteen derivatives for anticancer activity. Eleven them demonstrated potent activity against both liver (HepG2) adenoc...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2001
ali khalafi nezhad aboulghasem hashemi

efficient knoevenagel condensation of barbituric acid with different aromatic aldehydes on basic alumina was performed in a conventional microwave over in the absence of solvent.

2011
Maral Shekarchi Latifeh Navidpour Afshin Rajabi Khorami Mahtab shekarchi Alireza Partoazar Hamed Shafaroodi Narges Rahmanipour Abbas Shafiee Maryam Shekarchi

Diclofenac sodium has been used for its anti-inflammatory actions for about 28 years, but since all the non-steroidal anti-inflammatory drugs (NSAIDs) suffer from the lethal gastro intestinal (GI) toxicities, diclofenac sodium is not an exception. The free -COOH group is thought to be responsible for the GI toxicity associated with all traditional NSAIDs. In the present research, the main motto...

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