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Articles 8521 - 8550 of 15571
Full-Text Articles in Entire DC Network
Total Synthesis Of Ht-13-A And Ht-13-B, Total Synthesis Of Aurantioclavine, Progress Towards The Synthesis Of Cycloclavine, Yilin Zhang
Graduate Theses, Dissertations, and Problem Reports (ETD)
Total synthesis of tetracyclic indole alkaloid ht-13-A and ht-13-B has been accomplished from commercially available (S)-4-amino-2-hydroxybutyric acid and trans4-hydroxy-L-proline respectively. The key synthetic steps include an acyliminium ion allylation, a Mitsunobu reaction, a palladium-catalyzed Stille-Kelly cross coupling reaction, and a carbon monoxide mediated palladium-catalyzed reductive Nheterocyclization. The total synthesis of aurantioclavine has been studied. The synthesis commenced with 2-amino-3-nitrophenol. Key synthetic steps include a Stille coupling reaction, a Heck reaction, a Lewis acid mediated cyclization and a carbon monoxide mediated palladium-catalyzed reductive N-heterocyclization. In addition, the first asymmetric total synthesis of (+)-cycloclavine has been studied. Key synthetic steps include a …
A Convenient Route For The Synthesis Of New Thiadiazoles, Abdelwahed Sayed, Yasser Zaki, Emad Aish
A Convenient Route For The Synthesis Of New Thiadiazoles, Abdelwahed Sayed, Yasser Zaki, Emad Aish
Turkish Journal of Chemistry
The present work describes the preparation of new thiadiazoles through a simple intramolecular reaction of mono- and bis-hydrazonoyl halides with methyl hydrogen phenyl carbonimidodithioate or methyl-2-arylidene hydrazinecarbodithioate. The synthetic method involves nucleophilic substitution followed by intramolecular cyclization reactions mediated by evolution of methanethiol. The structures of the title compounds were elucidated by elemental analyses, and FTIR, MS and NMR spectra.
Synthesis And Evaluation Of Some Novel Thiazoles And 1,3-Thiazines As Potent Agents Against The Rabies Virus, Magda Abdalla, Sobhi Gomha, Mohamad Abd Elaziz, Nany Serag
Synthesis And Evaluation Of Some Novel Thiazoles And 1,3-Thiazines As Potent Agents Against The Rabies Virus, Magda Abdalla, Sobhi Gomha, Mohamad Abd Elaziz, Nany Serag
Turkish Journal of Chemistry
A series of novel thiazoles and 1,3-thiazine derivatives were synthesized in good yield via reaction of ethyl 3-(1-(2-thiocarbamoylhydrazono)ethyl)-1,5-diphenyl-1$H$-pyrazole-4-carboxylate with hydrazonoyl halides and arylidenemalononitriles, respectively. The structure of the newly synthesized products was elucidated via elemental analysis, spectral data, and alternative routes whenever possible. Moreover, the antiviral screening of the products was evaluated and the results revealed that some of them have strong to moderate potency against the rabies virus compared with the reference drug.
Synthesis, Reaction, And Evaluation Of The Anticancer Activity Of 6,7,8,9-Tetrahydro-5$H$-Cyclohepta[4,5]Selenopheno[2,3-$D$]Pyrimidine Derivatives, Kadi̇r Doğanay, Ünzi̇le Keleştemur, Sevgi̇ Balcioğlu, Burhan Ateş, Ali̇ye Altundaş
Synthesis, Reaction, And Evaluation Of The Anticancer Activity Of 6,7,8,9-Tetrahydro-5$H$-Cyclohepta[4,5]Selenopheno[2,3-$D$]Pyrimidine Derivatives, Kadi̇r Doğanay, Ünzi̇le Keleştemur, Sevgi̇ Balcioğlu, Burhan Ateş, Ali̇ye Altundaş
Turkish Journal of Chemistry
The cyclocondensation of 2-amino-5,6,7,8-tetrahydro-4$H$-cyclohepta[$b$] selenophene-3-carbonitrile (1) with formic acid and formamide gave the selenophenopyrimidine 15 and selenophenopyrimidone 6 derivatives. The reaction of 6 with phosphorus oxychloride produced 4-chloro-6,7,8,9-tetrahydro-5$H$-cyclohepta[4,5] seleno[2,3-$d$]pyrimidine (12), the key compound for our nucleophilic substitution reactions. The hydrazinoselenophenopyrimidine 19 obtained from the reaction of 12 with hydrazine hydrate was converted to its tetrazoloselenophenopyrimidine 21 and triazoloselenophenopyrimidine 26 derivatives. Moreover, the chloropyrimidine derivative was reacted with pyrrolidine and morpholine to afford 4-(1-pyrrolidinyl)-6,7,8,9-tetrahydro-5$H$-cylohepta[4,5]selenopheno[2,3-$d$]pyrimidine (27) and 4-(6,7,8,9-tetrahydro-5$H$-cyclohepta[4,5]selenopheno[2,3-$d$]pirimidin-4-yl)morpholine (28). Anticancer activities of the synthesized compounds were investigated against the MCF-7 breast cancer cell line and the IC$_{50}$ values of these compounds were …
Adsorption Of Cellulase On Poly(2-Hydroxyethyl Methacrylate) Cryogels Containing Phenylalanine, Murat Yavuz, Oğuz Çakir, Zübeyde Baysal
Adsorption Of Cellulase On Poly(2-Hydroxyethyl Methacrylate) Cryogels Containing Phenylalanine, Murat Yavuz, Oğuz Çakir, Zübeyde Baysal
Turkish Journal of Chemistry
The aim of this study was to prepare a supermacroporous cryogel that can be used for the adsorption of cellulase. The macroporous cryogel of poly(2-hydroxyethyl methacrylate-N-methacryloyl-l-phenylalanine) [p(HEMA-MAPA)] was prepared by copolymerization of 2-hydroxyethyl methacrylate (HEMA) with a functional monomer of N-methacryloyl-l-phenylalanine (MAPA). The cryogel was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and swelling tests. The effects of several parameters such as medium pH, temperature, ionic strength, and flow rate on cellulase adsorption were also investigated. Maximum cellulase adsorption was observed at 25 $^{\circ}$C and pH 4.0. Furthermore, adsorbed cellulase was desorbed from the cryogel by using 1.0 …
Electrochemical Investigation Of2-[8-Hydroxyquinoline-5-Yl)Azo]Benzo[$C$]Cinnoline On A Platinum Electrode In Dimethysulfoxide, Funda Öztürk, Zehra Yazan, Oznur Olmez, Emi̇ne Kiliç, Esma Kiliç
Electrochemical Investigation Of2-[8-Hydroxyquinoline-5-Yl)Azo]Benzo[$C$]Cinnoline On A Platinum Electrode In Dimethysulfoxide, Funda Öztürk, Zehra Yazan, Oznur Olmez, Emi̇ne Kiliç, Esma Kiliç
Turkish Journal of Chemistry
2-[8-hydroxyquinoline-5-yl)azo]benzo[c]cinnoline was synthesized for the first time and shown to possess electrochromic characteristic, i.e. changing color during the forward and back electrolysis at --1.35 V and 0.00 V, respectively, in DMSO medium. Therefore, the electrochemical investigation of this compound appears to be worthwhile. The electrochemical reduction of 2-[8-hydroxyquinoline-5-yl)azo]benzo[c]cinnoline was investigated by cyclic voltammetry, controlled potential electrolysis, and chronoamperometry techniques in the presence of 0.10 mol L$^{-1}$ tetrabutylammonium tetrafluoroborate in dimethyl sulfoxide at platinum electrode. 2-[8-Hydroxyquinoline-5-yl)azo]benzo[c] cinnoline displays three sharp cathodic peaks and three anodic peaks in the cyclic voltammogram. The diffusion coefficients and the number of electrons transferred were calculated …
Latest Trends, Green Aspects, And Innovations In Liquid-Phase--Based Microextraction Techniques: A Review, Erkan Yilmaz, Mustafa Soylak
Latest Trends, Green Aspects, And Innovations In Liquid-Phase--Based Microextraction Techniques: A Review, Erkan Yilmaz, Mustafa Soylak
Turkish Journal of Chemistry
Liquid-phase microextraction (LPME) methods including single-drop microextraction (SDME), hollow-fiber LPME (HF-LPME), and dispersive liquid-liquid microextraction (DLLME) have in the very short time since their invention grabbed the attention of scientists. Up to now, LPME methods have shown important innovations for the extraction and preconcentration of both inorganic and organic trace analytes from different matrices. These LPME methods offer unique advantages such as high preconcentration factor for target analytes in a single step, low cost, simplicity, excellent preconcentration capability, sample cleanup and integration of steps, and combined use with almost every analytical measurement technique. We describe the milestones and the combined …
Chromium Redox Speciation In Food Samples, Krystyna Pyrzynska
Chromium Redox Speciation In Food Samples, Krystyna Pyrzynska
Turkish Journal of Chemistry
Chromium is an element with important biological characteristics, depending on its different species. Cr(III) is considered as essential; however, the Cr(VI) form is classified as carcinogenic.~For this reason, speciation analysis in food samples is a very important question. The proposed data procedures for chromium redox speciation in the literature can be divided into those with the use of online hyphenated techniques and those where appropriate sample pretreatment is necessary. The strategies for nonchromatographic speciation are mainly based on selective liquid--liquid extraction procedures, coprecipitation, selective separation of chromium species using a solid phase extraction column, or complexation reactions. In this paper, …
Polyacrylamide And Its Derivatives For Oil Recovery, Zun Chen
Polyacrylamide And Its Derivatives For Oil Recovery, Zun Chen
Doctoral Dissertations
"Polyacrylamide is an umbrella term used to describe the homo-polymer of acrylamide and the copolymer of acrylamide with a small amount of other monomers. Owing to their superior property on increasing viscosity and gelling ability in the presence of crosslinkers, polyacrylamides has become the primarily selection for polymer flooding and gel treatment agent in enhanced oil recovery. Recent developments, performance, applications and limitations of polyacrylamides and its derivatives, including copolymers and hydrogels for enhancing oil recovery are reviewed.
A water-free suspension system was developed to synthesize PAMs and PAMs-microgel. Products are dry particle powder and ready to disperse in water. …
Bioactivity/Cytotoxicity Of Micro-/Nano-Materials And Novel Development Of Fiber-Optic Probes For Single Cell Monitoring, Qingbo Yang
Doctoral Dissertations
"Manufactured nano-/micro-materials (MNMs) have been widely used and their interactions with niche biological environment are highly concerned for both of their biohazardous and bioactive effects, whereas no available comprehensive evaluations or regulations have been provided yet. This dissertation thus focuses on three major aspects: 1) fundamental toxicity understandings of a typical MNMs (zinc oxide nanoparticles), 2) bioactivity evaluations of representative bioactive MNMs, and 3) development of novel micro-probes for high spatial resolution monitoring. Firstly, the NP's concentration, irradiation, hydrodynamic size, and the localized pH, ionic strength, NP zeta-potential as well as dissolved oxygen levels were found correlated with the production …
Continuous Flow Reactor For Carbonic Acid Hydrolysis/Pretreatment Of Microalgal Biomass To Produce Bioethanol, Nicholas Dudenhoeffer
Continuous Flow Reactor For Carbonic Acid Hydrolysis/Pretreatment Of Microalgal Biomass To Produce Bioethanol, Nicholas Dudenhoeffer
Doctoral Dissertations
"In order to maximize bioethanol production an efficient pretreatment method for the hydrolysis of polysaccharides to fermentable sugars is necessary. Commonly used pretreatment methods are the slow enzymatic hydrolysis and the corrosive mineral acid hydrolysis process that requires a post-treatment neutralization step and generates waste stream. We investigated the high temperature water with carbonic acid catalyst as an alternative method. Carbonic acid generated from dissolved CO2 is inexpensive and environmentally benign, and easily removed by decompression. A high pressure continuous flow reactor that can continuously process the wet biomass stream and perform the carbonic acid hydrolysis in-situ using the …
Synthesis And Functionalization Of A Triaryldiamine-Base Photoconductive/Photorefractive Composite, And Its Application To Aberrated Image Restoration, Yichen Liang
Doctoral Dissertations
"Organic photorefractive (PR) composites have recently emerged as an important class of materials for applications including high-density data storage, optical communication, and biomedical imaging. In an effort to further improve their performance, this study focused on the utilization of functionalized semiconductor nanocrystals to photosensitize triaryamine (TPD)-based PR composites, as well as the application of TPD-based PR composites in the restoration of aberrated optical information. A novel approach to functionalize CdSe quantum dot (QCdSe) was firstly introduced where the sulfonated triarydiamine (STPD) was used as charge-transporting ligand to passivate QCdSe. TPD-based photoconductive and PR composites were photosensitized with the STPD-passivated QCdSe …
Square Wave Voltammetric Determination Of Valproic Acid In Pharmaceutical Preparations, Ebru Türköz Acar, Ati̇ye Nur Onar
Square Wave Voltammetric Determination Of Valproic Acid In Pharmaceutical Preparations, Ebru Türköz Acar, Ati̇ye Nur Onar
Turkish Journal of Chemistry
The electrochemical behavior of valproic acid (VAL) was investigated using square wave voltammetry, cyclic voltammetry, and sampled direct current polarography and a new square wave voltammetric method was developed for determination of VAL in pharmaceutical preparations. VAL showed two reduction peaks at about --0.2 V and --0.8 V vs. Ag/AgCl 3 M KCl with a hanging mercury drop electrode in 0.05 M pH 3.3 Britton--Robinson (BR) buffer. These peaks were named peak I and peak II, respectively. The types of limiting current of both peaks were determined as diffusion controlled based on cyclic voltammetry studies. A linear calibration graph was …
Synthesis And Structural Properties Of $N$-3,4-(Dichlorophenyl)-3-Oxo-3- Phenyl-2-(Phenylcarbonyl)Propanamide And Its Cu(Ii) Complex, Ahmet Oral Sarioğlu, Tuğba Taşkin Tok, Mehmet Akkurt, Muhammad Nawaz Tahir, Mehmet Sönmez
Synthesis And Structural Properties Of $N$-3,4-(Dichlorophenyl)-3-Oxo-3- Phenyl-2-(Phenylcarbonyl)Propanamide And Its Cu(Ii) Complex, Ahmet Oral Sarioğlu, Tuğba Taşkin Tok, Mehmet Akkurt, Muhammad Nawaz Tahir, Mehmet Sönmez
Turkish Journal of Chemistry
A new N-carboxamide compound (3) was synthesized by the reaction of dibenzoylaceticacid-$N$-carboxyethyla\-mide (1) and 3,4-dichloroaniline (2). The $N$-(3,4-dichlorophenyl)-3-oxo-3-phenyl-2-(phenylcarbonyl) propanamide (3) subsequently reacted with Cu salt to produce its Cu(II) complex compound (4). The compounds were characterized by analytical and spectral methods. In addition, X-ray diffraction was performed to characterize and obtain detailed information about the structure of 3. The fully optimized geometries of compounds 3 and 4 were calculated at different basis sets by using the Gaussian09 (G09) software to investigate their 3D geometries and electronic structures. Comparisons between the calculated and experimental data including molecular structures, fundamental vibrational modes, …
Liquid State $^{15}$N Nmr Studies Of $^{15}$N Isotope Labeled Phthalocyanines, Armağan Atsay, Ahmet Gül, Makbule Koçak
Liquid State $^{15}$N Nmr Studies Of $^{15}$N Isotope Labeled Phthalocyanines, Armağan Atsay, Ahmet Gül, Makbule Koçak
Turkish Journal of Chemistry
$^{15}$N labeled soluble metallo- and metal-free phthalocyanines are described for the first time. The complexes were synthesized starting from phthalic anhydride derivatives using 98{\%} $^{15}$N enriched urea. The effects of the substitution pattern, aggregation, and coordinated metal on $^{15}$N chemical shifts in liquid state NMR were studied.
Wittig--Horner Reagents: Powerful Tools In The Synthesis Of 5-And 6-Heterocyclic Compounds; Shedding Light On Their Application In Pharmaceutical Chemistry, Rizk Elsayed Khidre, Wafaa Mahmoud Abdou
Wittig--Horner Reagents: Powerful Tools In The Synthesis Of 5-And 6-Heterocyclic Compounds; Shedding Light On Their Application In Pharmaceutical Chemistry, Rizk Elsayed Khidre, Wafaa Mahmoud Abdou
Turkish Journal of Chemistry
This paper reviews literature over 25 years' activity on phosphoryl carbanion reagents and shows that these compounds are powerful tools in organic chemistry. The main target of this review is to outline some of the reactive peculiarities that make this class of compounds powerful tools in the synthesis of 5- and 6-heterocyclic compounds and/or substituted heterocycle phosphor esters. The importance of these latter compounds in pharmacology is also discussed.
Synthetic Approaches Towards The Synthesis Of Beta-Blockers (Betaxolol, Metoprolol, Sotalol, And Timolol), Furqan Ahmad Saddique, Ameer Fawad Zahoor, Muhammmad Yousaf, Muhammmad Irfan, Matloob Ahmad, Asim Mansha, Zulfiqar Ali Khan, Syed Ali Raza Naqvi
Synthetic Approaches Towards The Synthesis Of Beta-Blockers (Betaxolol, Metoprolol, Sotalol, And Timolol), Furqan Ahmad Saddique, Ameer Fawad Zahoor, Muhammmad Yousaf, Muhammmad Irfan, Matloob Ahmad, Asim Mansha, Zulfiqar Ali Khan, Syed Ali Raza Naqvi
Turkish Journal of Chemistry
Numerous efficient synthetic methodologies have been elaborated for the synthesis of $\beta $-blockers since the introduction of propranolol (a beta-blocker) in 1968. In this review, focus is placed on the more concise asymmetric and bioenzymatic synthetic approaches attempted towards the synthesis of beta-blockers (betaxolol, metoprolol, sotalol, and timolol).
Synthetic Access To Some New Benzothiazole-Based 1,3,4-Thiadiazole And 1,3-Thiazole Derivatives, Kamal M. Dawood, Eman A. Ragab, Korany A. Ali
Synthetic Access To Some New Benzothiazole-Based 1,3,4-Thiadiazole And 1,3-Thiazole Derivatives, Kamal M. Dawood, Eman A. Ragab, Korany A. Ali
Turkish Journal of Chemistry
1-(Benzothiazol-2-yl)-3-phenylthiourea\textbf{ 2} was prepared and treated with hydrazonoyl chlorides \textbf{3a}--\textbf{e }to yield the corresponding 5-(benzothiazol-2-ylimino)-1,3,4-thiadiazole derivatives \textbf{6a}--\textbf{e}, respectively. Reaction of the thiourea derivative \textbf{2} with ethyl 2-chloro-3-oxobutanoate \textbf{9} afforded the corresponding 2-(benzothiazol-2-ylimino)thiazole-5-carboxylate derivative \textbf{11}. The newly synthesized heterocyclic derivatives were confirmed from their elemental and spectral analyses.
Heterogeneous Fenton-Like Degradation Of Acid Red 17 Using Fe-Impregnated Nanoporous Clinoptilolite: Artificial Neural Network Modeling And Phytotoxicological Studies, Alireza Khataee, Mehrangiz Fathinia, Soghra Bozorg
Heterogeneous Fenton-Like Degradation Of Acid Red 17 Using Fe-Impregnated Nanoporous Clinoptilolite: Artificial Neural Network Modeling And Phytotoxicological Studies, Alireza Khataee, Mehrangiz Fathinia, Soghra Bozorg
Turkish Journal of Chemistry
Heterogeneous Fenton-like removal of Acid Red 17 (AR17) from aqueous solution was investigated. Fe-impregnated nanoporous clinoptilolite (Fe-NP-Clin) was prepared by an impregnation method and used as a catalyst. A complete characterization including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), inductively coupled plasma (ICP), and Brunauer--Emmett--Teller (BET) analyses was done to describe the physical and chemical properties of NP-Clin and Fe-NP-Clin samples. The effects of five operational parameters, i.e. solution pH, H$_{2}$O$_{2}$ dosage, catalyst loading, AR17 concentration, and reaction time, on the removal efficiency of AR17 were studied. For the first time, an artificial neural network …
Polybrominated Methoxy- And Hydroxynaphthalenes, Kiymet Berki̇l Akar, Osman Çakmak, Tuncay Tunç
Polybrominated Methoxy- And Hydroxynaphthalenes, Kiymet Berki̇l Akar, Osman Çakmak, Tuncay Tunç
Turkish Journal of Chemistry
Regio- and stereoselective synthesis are described for convenient preparation of hydroxy- and methoxynaphthalenes starting from naphthalene (\textbf{1}). \textit{cis,cis,trans}-2,3,5,8-Tetrabromo-4-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol (\textbf{6}), \textit{cis,cis,trans}-2,3,5,8-tetrabromo-1,4-dimethoxy-1,2,3,4-tetrahydronaphthalene (\textbf{7}), and \textit{cis,cis,cis}-2,3,5,8-tetrabromo-1,4-dimethoxy-1,2,3,4-tetrahydronaphthalene (\textbf{8}) were obtained with silver-induced substitution of \textit{trans,cis,trans}-1,2,3,4, 5,8-hexabromo-1,2,3,4-tetrahydronaphthalene (\textbf{3}). Base-promoted aromatization of dimethoxides \textbf{7} and \textbf{8} afforded 3,5,8-tribromo-1-methoxynaphthalene (\textbf{9}) and 2,5,8-tribromo-1-methoxynaphthalene (\textbf{10}). The reaction of \textbf{6 }with sodium methoxide formed compounds \textbf{10 }and 3,5,8-tribromonaphthalen-1-ol (\textbf{16}). Bromination of \textbf{9} and\textbf{ 16} with Br$_{2}$ in dichloromethane at room temperature produced 2,3,5,8-tetrabromo-1-methoxynaphthalene (\textbf{14}) and 2,3,4,5,8-pentabromonaphthalen-1-ol (\textbf{18}), respectively, while compound \textbf{10} did not react in the same conditions. Pyridine-induced elimination of hexabromide \textbf{3} afforded 1,4,6\textbf{-}tribromnaphthalene (\textbf{21}) in 99{\%} yield and …
New Antimicrobial Biscembrane Hydrocarbon And Cembranoid Diterpenes From The Soft Coral Sarcophyton Trocheliophorum, Muhammad Zubair, Walied Alarif, Khalid Al-Footy, Mohamed Ph, Magda Ali, Salim Basaif, Sultan Al-Lihaibi, Seif-Eldin Ayyad
New Antimicrobial Biscembrane Hydrocarbon And Cembranoid Diterpenes From The Soft Coral Sarcophyton Trocheliophorum, Muhammad Zubair, Walied Alarif, Khalid Al-Footy, Mohamed Ph, Magda Ali, Salim Basaif, Sultan Al-Lihaibi, Seif-Eldin Ayyad
Turkish Journal of Chemistry
A new tetracyclic biscembrane hydrocarbon, trocheliane (1), along with two new cembranoid diterpenes, sarcotrocheldiol A (2) and B (3), and the known diterpene cembrene-C (4), were isolated from the Red Sea soft coral Sarcophyton trocheliophorum. The structures and relative stereochemistry of the compounds were elucidated by interpretation of MS, 1 D NMR, and 2 D NMR experiments. The sensitivity of some pathogenic bacteria used as test organisms to the new compounds 1-3 was determined. 1 showed appreciable antimicrobial activity with the diameter of inhibition zones ranging from 11 to 18 mm. 1 was active against the two multidrug resistant bacteria …
Synthesis And Evaluation Of Novel $N,N'$-Disubstituted Benzimidazolium Bromides Salts As Antitumor Agents, Hasan Küçükbay, Akin Mumcu, Suat Teki̇n, Süleyman Sandal
Synthesis And Evaluation Of Novel $N,N'$-Disubstituted Benzimidazolium Bromides Salts As Antitumor Agents, Hasan Küçükbay, Akin Mumcu, Suat Teki̇n, Süleyman Sandal
Turkish Journal of Chemistry
Novel benzimidazolium bromides salts having (4-methoxyphenyl)ethyl, (phthalimide-2-yl)methyl, 4-nitro- benzyl, 2-phenylethyl, penthyl, or allyl groups were synthesized and their characterizations were conducted by $^{1}$H and $^{13}$C NMR and IR spectroscopic methods, and microanalysis. In vitro antitumor activities of the novel benzimidazole compounds (1-7) were determined by using ovarian (A2780) and prostate (PC-3) cancer cell lines. Antitumor properties of all compounds were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. A time-dependent cell viability assay for the tested benzimidazole compounds was performed and the IC$_{50}$ values of the compounds were calculated after treatment for 24 and 48 h. Our results indicate that the tested …
Synthesis And Application Of Polyvinylimidazole-Based Bronsted Acidic Ionic Liquid Grafted Silica As An Efficient Heterogeneous Catalyst In The Preparation Of Quinoxaline Derivatives, Bahman Tamami, Alireza Sardarian, Elaheh Ataollahi
Synthesis And Application Of Polyvinylimidazole-Based Bronsted Acidic Ionic Liquid Grafted Silica As An Efficient Heterogeneous Catalyst In The Preparation Of Quinoxaline Derivatives, Bahman Tamami, Alireza Sardarian, Elaheh Ataollahi
Turkish Journal of Chemistry
Two types of polymer-grafted silica based on polyvinylimidazole Bronsted acidic ionic liquids were prepared and used as new heterogeneous catalysts for the preparation of pharmaceutically important quinoxaline derivatives. These catalysts were characterized by thermogravimetric analysis, FT-IR spectroscopy, and titration. They could be recycled without considerable loss in their catalytic activity. High efficiency of the catalysts along with short reaction times, high yields, easy purification, recyclability, and simple procedure are among the advantages of these catalytic systems.
An Efficient One-Pot, Three-Component Synthesis Of 6-Cyano-Hexahydro-4$H$-Thieno[3',2':5,6]Pyrimido[1,2-$A$]Quinoline-2-Carboxylates And Their Spiro Derivatives From $\Beta $-Enaminones, Said Ahmed Soliman Ghozlan, Doaa Mohmed Abdelmoniem, Amr Mohmed Abdelmoniem, Ismail Abdelshafy Abdelhamid
An Efficient One-Pot, Three-Component Synthesis Of 6-Cyano-Hexahydro-4$H$-Thieno[3',2':5,6]Pyrimido[1,2-$A$]Quinoline-2-Carboxylates And Their Spiro Derivatives From $\Beta $-Enaminones, Said Ahmed Soliman Ghozlan, Doaa Mohmed Abdelmoniem, Amr Mohmed Abdelmoniem, Ismail Abdelshafy Abdelhamid
Turkish Journal of Chemistry
A simple and efficient one-pot synthesis of novel thieno[3',2':5,6]pyrimido[1,2-a]quinoline-2-carboxylates (5a-d) and their spirooxindole derivatives (12a-d) was accomplished. Thus, the Michael addition reaction of the cyclic $\beta $-enaminone 3 with the corresponding $\alpha ,\beta $-unsaturated nitrile derivatives 4a-d in refluxing EtOH in the presence of piperidine afforded 5a-d in good yields. On the other hand, spirooxindole derivatives 12a-d were synthesized by the reaction of cyclic $\beta $-enaminone 3 with the corresponding 3-cyanomethylidene-2-oxoindoles 11a-d in refluxing EtOH.
Synthesis, And Prediction Of Molecular Properties And Antimicrobial Activity Of Some Acylhydrazones Derived From $N$-(Arylsulfonyl)Methionine, Esra Tatar, Sevi̇l Şenkardeş, Hasan Erdi̇nç Selli̇tepe, Şükri̇ye Güni̇z Küçükgüzel, Şengül Alpay Karaoğlu, Ari̇f Bozdeveci̇, Erik De Clercq, Christophe Pannecouque, Tai̇bi̇ Ben Hadda, İlkay Küçükgüzel
Synthesis, And Prediction Of Molecular Properties And Antimicrobial Activity Of Some Acylhydrazones Derived From $N$-(Arylsulfonyl)Methionine, Esra Tatar, Sevi̇l Şenkardeş, Hasan Erdi̇nç Selli̇tepe, Şükri̇ye Güni̇z Küçükgüzel, Şengül Alpay Karaoğlu, Ari̇f Bozdeveci̇, Erik De Clercq, Christophe Pannecouque, Tai̇bi̇ Ben Hadda, İlkay Küçükgüzel
Turkish Journal of Chemistry
A series of 38 new acylhydrazones [3-40], derived from (2$S)$-4-(methylsulfanyl)-2-[[(4-methylphenyl)sulfonyl] amino]butanoic acid hydrazide [2], were synthesized and evaluated for their anti-HIV and antimicrobial activity with the further aim to develop acylhydrazones carrying an amino acid side chain. All tested compounds possess stronger activity against gram (+) bacteria. Compound 23 was found active against methicillin-resistant Staphylococcus aureus (MRSA) with a MIC value of 3.9 $\mu $g/mL. The MIC value of compound 30 against Enterococcus faecalis, Listeria monocytogenes, and Bacillus cereus was 8 $\mu $g/mL. A computational study for prediction of ADME and drug-like properties (solubility, drug-likeness, and drug score) as well …
Comparative Density Functional Study Of Antioxidative Activity Of The Hydroxybenzoic Acids And Their Anions, Zoran Markovic, Jelena Djorovic, Jasmina M. Dimitric Markovic, Radomir Biocanin, Dragan Amic
Comparative Density Functional Study Of Antioxidative Activity Of The Hydroxybenzoic Acids And Their Anions, Zoran Markovic, Jelena Djorovic, Jasmina M. Dimitric Markovic, Radomir Biocanin, Dragan Amic
Turkish Journal of Chemistry
Hydroxybenzoic acids (HBAs) and their anions play an important role in the food and pharmaceutical industries because of their antioxidant activity. In this study, we examined the mechanisms of the free radical scavenging action of HBAs and their anions using density functional theory (DFT) methods. Reaction enthalpies related to the mechanisms of free radical scavenging by the investigated species were calculated by DFT methods in water, DMSO, pentylethanoate, and benzene. Hydrogen atom transfer (HAT) is a preferred reaction pathway in benzene, while sequential proton loss electron transfer (SPLET) is a predominant reaction pathway in polar solvents, water, and DMSO for …
Ecofriendly One-Pot Synthesis And Antiviral Evaluation Of Novel Pyrazolyl Pyrazolines Of Medicinal Interest, Sobhi Gomha, Magda Abdalla, Mohamad Abd El-Aziz, Nany Serag
Ecofriendly One-Pot Synthesis And Antiviral Evaluation Of Novel Pyrazolyl Pyrazolines Of Medicinal Interest, Sobhi Gomha, Magda Abdalla, Mohamad Abd El-Aziz, Nany Serag
Turkish Journal of Chemistry
Ethyl 3-acetyl-1,5-diphenyl-1$H$-pyrazole-4-carboxylate reacts with a variety of arylaldehydes by grinding method in the presence of a catalytic amount of sodium hydroxide at ambient temperature to give the respective chalcones. The latter compounds react also by grinding method with nitrogen nucleophiles such as hydrazine hydrate, phenylhydrazine, and thiosemicarbazide to afford the corresponding pyrazol-3-yl pyrazolines. A series of 6-pyrazolylpyrimidine-2-thione derivatives were prepared by reaction of the above chalcones with thiourea by grinding method in the presence of a catalytic amount of sodium hydroxide at room temperature. In addition, 7-pyrazolylpyridopyrimidine-3-thione was prepared by reaction of chalcone with 6-aminothiouracil. All the newly synthesized compounds …
Visible Light Photocatalysis Of A Textile Dye Over Zno Nanostructures Covered On Natural Diatomite, Reza Darvishi Cheshmeh Soltani, Zohreh Haghighat
Visible Light Photocatalysis Of A Textile Dye Over Zno Nanostructures Covered On Natural Diatomite, Reza Darvishi Cheshmeh Soltani, Zohreh Haghighat
Turkish Journal of Chemistry
In the present study, ZnO nanostructures were ultrasonically synthesized and immobilized on the surface of diatomite and used for visible light photocatalysis of Acid Red 88 (AR88) in the aqueous phase. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses were employed for characterization of the samples. The process was optimized via response surface methodology (RSM) on the basis of central composite design (CCD). Based on numerical optimization, for the maximized color removal of 96% the initial dye concentration, the catalyst dosage, the reaction time, and the initial pH were 13 mg/L, 1.5 g/L, 85 min, and 4, respectively. The …
Prostereoisomerism And Biological Activity: Possible Implications For Drug Design, Sosale Chandrasekhar
Prostereoisomerism And Biological Activity: Possible Implications For Drug Design, Sosale Chandrasekhar
Turkish Journal of Chemistry
Prostereoisomerism (PIM), representing a subgroup within the achiral class of molecules, is manifested in a chiral environment. Although this is regardless of the orientation of the prostereoisomeric (PIC) molecule, PIM is manifested most emphatically in relation to a chiral surface (`two-dimensional chirality'). Then PIM is tantamount to `de facto chirality' as attachment of the PIC molecule to the surface leads to diastereomeric possibilities (cf. Ogston's hypothesis). Furthermore, the formation of host--guest complexes requires a steric complementarity between the component molecules. The fact that the weak dispersive forces involved therein require an optimum distance implies a `snugness of fit' criterion. This …
Synthesis Of Novel Thiazolylpyrazoline Derivatives And Evaluation Of Their Antimicrobial Activities And Cytotoxicities, Aouatef Tabbi, Zafer Asim Kaplancikli, Dahmane Tebbani, Leyla Yurttaş, Zerri̇n Cantürk, Özlem Atli, Merve Baysal, Gülhan Turan Zitouni
Synthesis Of Novel Thiazolylpyrazoline Derivatives And Evaluation Of Their Antimicrobial Activities And Cytotoxicities, Aouatef Tabbi, Zafer Asim Kaplancikli, Dahmane Tebbani, Leyla Yurttaş, Zerri̇n Cantürk, Özlem Atli, Merve Baysal, Gülhan Turan Zitouni
Turkish Journal of Chemistry
Several novel thiazolylpyrazoline derivatives were synthesized by reacting substituted 3,5-diaryl-1-thiocarba\-moyl-2-pyrazolines with phenacylbromides. The structures of the synthesized compounds were confirmed by IR, $^{1}$H NMR, $^{13}$C NMR, and MS spectral data. Their antimicrobial activities against Staphylococcus aureus(ATCC-25923), Enterococcus faecalis} (ATCC-29212), Enterococcus faecalis (ATCC-51922), Listeria monocytogenes (ATCC-1911), Klebsiella pneumoniae (ATCC-700603), Pseudomonas aeruginosa (ATCC-27853), Escherichia coli (ATCC-35218), Escherichia coli (ATCC-25922), Candida albicans (ATCC-90028), Candida glabrata (ATCC-90030), Candida krusei (ATCC-6258), and Candida parapsilosis (ATCC-22019) were investigated. The compounds were also studied for their cytotoxic effects using a MTT assay. Compound 7c showed the highest antimicrobial activity, possessing the same potential as chloramphenicol against K. …