Auswahl der wissenschaftlichen Literatur zum Thema „Alkylated thiazine“

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Zeitschriftenartikel zum Thema "Alkylated thiazine"

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Ahmed, S., and S. K. Saha. "Electrochemical study of the reaction between progressively alkylated thiazine leucodyes and Fe(III) on a glassy carbon electrode." Canadian Journal of Chemistry 74, no. 10 (1996): 1896–902. http://dx.doi.org/10.1139/v96-213.

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An electrochemical investigation on five progressively alkylated thiazine dyes in the presence of Fe(III) ions is reported. The theory of the catalytic regeneration mechanism involving an electrode reaction followed by a coupled chemical reaction is applied to derive kinetic parameters of homogeneous reaction. The second-order rate constant for the reaction of thiazine leucodyes with Fe(III) ions was found to increase from 0.25 × 104 to 1.6 × 104 dm3 mol−1 s−1 upon monomethylation and to vary from 0.7 × 104 for the dimethyl derivative to 1.4 × 104 dm3mol−1 s−1 for the tetramethyl one. The elec
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Chakraborty, Amitabha, Shamsuzzaman Ahamed, Subrata Pal, and Swapan K. Saha. "Cyclic Voltammetric Investigations of Thiazine Dyes on Modified Electrodes." ISRN Electrochemistry 2013 (February 12, 2013): 1–7. http://dx.doi.org/10.1155/2013/959128.

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Electrochemical behavior of five progressively alkylated thiazine dyes has been investigated at glassy carbon/montmorillonite and glassy carbon/zeolite electrodes. Quantitative characteristics, associated with the positions of peak potentials (Ea and Ec) and current ratios (ia/ic), are measured with scan rates. The peak current observed in the modified electrodes is dependent on both the porosity and nature and number of sites involved in partitioning the complex into film. The values of diffusion coefficient for different dyes have been calculated from electrochemical data. It is suggested th
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Chakraborty, Amitabha, Samsuzzaman Ahmed, and Swapan K. Saha. "Electrochemical Studies of Progressively Alkylated Thiazine Dyes on a Glassy Carbon Electrode (GCE) in Water, Ethanol, and Triton X-100 Media†." Journal of Chemical & Engineering Data 55, no. 5 (2010): 1908–13. http://dx.doi.org/10.1021/je9009078.

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Fehlhammer, Wolf Peter, Hans Hoffmeister, Uwe Eckert, and Christian Robl. "Bor-stabilisierte Carbene, III [3 + 2]-Cycloadditionen an Borio-Nitrilylide / Boron-Stabilized Carbenes, III [3 + 2]-Cycloadditions to Borio Nitrile Ylides." Zeitschrift für Naturforschung B 48, no. 11 (1993): 1448–60. http://dx.doi.org/10.1515/znb-1993-1102.

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The borio nitrile ylides Li[Ph3B—C =N—CH—R] (R = CO2Et, Tos) react with various dipolarophiles regio- and site-specifically to give boron complexes of carbenoid five-membered heterocycles which have been alkylated in order to accomplish their isolation. Thus, isocyanates and isothiocyanates/trialkyloxonium salts give rise to the imidazoline-2-ylidene complexes 2-5, CS2/Et3O+ to the thiazoline-2-ylidene complex 6 and acetone/Et3O+ to the oxazoline-2-ylidene complexes 7a,b. Aryldiazonium ions are added regiospecifically in the “wrong” orientation that leads to mesoionic 1,2,4-triazolium-3-ato-tr
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Mohammed, Eman R., Manal Abdel Fattah Ezzat, Emad M. Seif, et al. "Synthesis of S-alkylated oxadiazole bearing imidazo[2,1-b]thiazole derivatives targeting breast cancer: In vitro cytotoxic evaluation and in vivo radioactive tracing studies." Bioorganic Chemistry 153 (December 2024): 107935. http://dx.doi.org/10.1016/j.bioorg.2024.107935.

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Ovonramwen, Oluwaseyi Bukky, Bodunde Joseph Owolabi, and Amowie Philip Oviawe. "Synthesis of (2Z)-4,6-Diphenyl-N-((2-(Piperidin-1-yl)Ethyl]-2H-1,3-Thiazin-2-Imino Hydrochloride and its Antimicrobial Activities." Asian Journal of Physical and Chemical Sciences, September 21, 2019, 1–9. http://dx.doi.org/10.9734/ajopacs/2019/v7i330096.

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Aim: The study aims to synthesize, characterize, and screen (2Z)-4,6-diphenyl-N-((2-(piperidin-1-yl)ethyl]-2H-1,3-thiazin-2-imino hydrochloride for microbial activities.
 Methodology: A (2Z)-4,6-diphenyl-N-((2-(piperidin-1-yl)ethyl]-2H-1,3-thiazin-2-imino hydrochloride was synthesized via two-steps reaction from chalcone using acetophenone and benzaldehyde, further cyclized with thiourea and later N-alkylated with 1-(2-chloroethyl)piperidine hydrochloride, its purity was tested by thin-layer chromatography (TLC) and characterized by Fourier transform infrared spectroscopy (FT-IR), proton
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Liu, Yufa, Junwei Liu, and Xiuming Liu. "Reaction of 2-thiazolidinethione with halohydrocarbon: synthesis of novel N-alkylated 2-thiazolidinethione and S-alkylated thiazoline derivatives." Heterocyclic Communications 16, no. 4-6 (2010). http://dx.doi.org/10.1515/hc.2010.015.

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Kaddouri, Yassine, Farid Abrigach, Sabir Ouahhoud, et al. "Mono-Alkylated Ligands Based on Pyrazole and Triazole Derivatives Tested Against Fusarium oxysporum f. sp. albedinis: Synthesis, Characterization, DFT, and Phytase Binding Site Identification Using Blind Docking/Virtual Screening for Potent Fophy Inhibitors." Frontiers in Chemistry 8 (December 11, 2020). http://dx.doi.org/10.3389/fchem.2020.559262.

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Twelve recent compounds, incorporating several heterocyclic moieties such as pyrazole, thiazole, triazole, and benzotriazole, made in excellent yield up to 37–99.6%. They were tested against Fusarium oxysporum f. sp. albedinis fungi (Bayoud disease), where the best results are for compounds 2, 4, and 5 with IC50 = 18.8–54.4 μg/mL. Density functional theory (DFT) study presented their molecular reactivity, while the docking simulations to describe the synergies between the trained compounds of dataset containing all the tested compounds (57 molecules) and F. oxysporum phytase domain (Fophy) enz
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Dissertationen zum Thema "Alkylated thiazine"

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Pal, Subrata. "Studies on physico - chemical characteristics of progressively alkylated thiazine dyes and their interaction with montmorillonite." Thesis, University of North Bengal, 1992. http://hdl.handle.net/123456789/715.

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Konferenzberichte zum Thema "Alkylated thiazine"

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Al-Jamal, Mazin H., Naeemah Al-Lami, and Ruqia M. Al-Azy. "Synthesis of new S, N, O-alkylated benzo [d] imidazo [2,1-b]thiazole and the study of their biological applications." In 2ND INTERNATIONAL CONFERENCE ON MATERIALS ENGINEERING & SCIENCE (IConMEAS 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0000174.

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