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Relevant bibliographies by topics / Thiazine

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Academic literature on the topic 'Thiazine'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Thiazine"

1

Slyvka, N. Yu, L. M. Saliyeva, E. M. Kadykalo, T. P. Bortnik, M. B. Litvinchuk, and M. V. Vovk. "Synthesis and growth regulatory activity of phenoxy substituted (benzo)imidazo[2,1-b][1,3]-thiazines." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 4 (July 2022): 61–68. http://dx.doi.org/10.32434/0321-4095-2022-143-4-61-68.

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A number of new 6-phenoxy-6,7-dihydro-5H-imidazo[2,1-b][1,3]thiazines 4a–g and their benzoannelated derivatives 4h–l were synthesized by the interaction of substituted 2-chlorobenzenes with 3-hydroxy(benzo)imidazo[2,1-b][1,3]thiazines in mild reaction conditions with the yields of 62–69%. The structure of the target compounds was proven by the results of 1H NMR and 13C NMR spectrometry and LC-MS. All newly synthesized compounds were studied for the features of the physiological development of seedlings of the dicotyledonous plant Cucumis sativus. According to the results of the experiment, it

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Yennawar, Hemant P., Saige L. Lowe, Matthew M. Mammen, Connor R. Verhagen, and Lee J. Silverberg. "Crystal structures of rac-2,3-diphenyl-2,3,5,6-tetrahydro-4H-1,3-thiazine-1,1,4-trione and N-[(2S,5R)-1,1,4-trioxo-2,3-diphenyl-1,3-thiazinan-5-yl]acetamide." Acta Crystallographica Section E Crystallographic Communications 79, no. 2 (2023): 120–23. http://dx.doi.org/10.1107/s2056989023000695.

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The syntheses and crystal structures of two thiazinone compounds, namely, rac-2,3-diphenyl-2,3,5,6-tetrahydro-4H-1,3-thiazine-1,1,4-trione, C16H15NO3S, in its racemic form, and N-[(2S,5R)-1,1,4-trioxo-2,3-diphenyl-1,3-thiazinan-5-yl]acetamide, C18H18N2O4S, in an enantiopure form, are reported. The thiazine rings in the two structures differ in their puckering, as a half-chair in the first and a boat pucker in the second. The extended structures for both compounds have only C—H...O-type interactions between symmetry-related molecules, and exhibit no π–π stacking interactions in spite of each ha

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B, Ravindar, Srinivasa Murthy M, and Afzal Basha Shaik. "DESIGN, FACILE SYNTHESIS, AND BIOLOGICAL EVALUATION OF NOVEL 1,3-THIAZINE DERIVATIVES AS POTENTIAL ANTICONVULSANT AGENTS." Asian Journal of Pharmaceutical and Clinical Research 9, no. 5 (2016): 272. http://dx.doi.org/10.22159/ajpcr.2016.v9i5.13676.

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ABSTRACTObjective: Chalcones and their heterocyclic analogs represent an important class of small molecules having anticonvulsant activities. Therefore, inthis study, the synthesis and anticonvulsant activity of some new chalcones and 1,3-thiazines were described.Methods: The reaction of 1-acetylnaphthalene with substituted aromatic aldehydes in the presence of aq. NaOH afforded corresponding chalconeswhich upon further cyclization with thiourea resulted in 1,3-thiazine derivatives. The newly synthesized compounds were tested for anticonvulsantactivity by pentylenetetrazole-induced seizures me

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Sarmad, Arsalan, Razia Sultana, and B. Syed Salman. "Synthesis, Characterize and Evaluation of anti-bacterial and anti-fungal activity of thiazines." International Journal of Research In Pharmaceutical Chemistry and Analysis 1, no. 1 (2019): 25–35. http://dx.doi.org/10.33974/ijrpca.v1i1.26.

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1,3 – Thiazines have been applied as useful starting materials in the stereo selective synthesis of compounds of pharmacological interest and they have served as chiral ligants and auxiliaries in enantioselective transformation. The thiazines are of great importance because they act as precursor for the synthesis of Cephalosporins (3,6-dihydro-2H-,1,3-thiazine) and then converted to the thiazine derivatives (an heterocyclic compounds). Therefore, it was thought to combine chalcones moiety to thiazine derivative together in a molecular frame work to see the biological activities, additive effor

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Slyvka, N. Yu, L. M. Saliyeva, M. B. Litvinchuk, A. M. Grozav, N. D. Yakovychuk, and M. V. Vovk. "Regioselective synthesis of new (imidazo[2,1-b] [1,3]-thiazin-6-yl)-1,2,3-triazole-5-carboxylates as potential antimicrobial agents." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 5 (October 2023): 114–22. http://dx.doi.org/10.32434/0321-4095-2023-150-5-114-122.

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The paper presents the results of the study on the interaction of azido(benz)imidazo[2,1-b][1,3]thiazines with acetylene carboxylates under non-catalytic conditions according to Huguesgen. It was established that the [3+2]-cyclocondensation of the specified reagents occurs regioselectively upon heating and without the use of a catalyst with the formation of a 1,4-addition product, alkyl 1-((benzo)imidazo[2,1-b][1,3]thiazine-6-yl)-1H-1,2,3-triazole-5-carboxylates 4a–g, the structure of which was thoroughly proved by the methods of 1H (13C) NMR spectroscopy and chromatography-mass spectrometry.

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Jawad, ASMAA, and Tamam Mahdi Salih. "Thiazine; Synthesis and Biological Activity." Al-Kufa University Journal for Biology 16, no. 3 (2024): 80–87. https://doi.org/10.36320/ajb/v16.i3.17436.

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Thiazines are a class of heterocyclic molecules that have not been extensively studied for their pharmacological effects. Various methods for synthesizing thiazine derivatives can be found in the literature. This review examines various techniques for synthesizing thiazines using environmentally friendly approaches. Thiazine derivatives are synthesized compounds that exhibit a wide range of biological activities, such as antibacterial, antifungal, antitumor, antimalarial, antineoplastic, antiviral, anti-inflammatory, analgesic, and anticancer properties. These compounds are considered a valuab

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Mohlala, Reagan L., Elena Mabel Coyanis, Muhammad Q. Fish, Manuel A. Fernandes, and Moira L. Bode. "Synthesis of 6-Membered-Ring Fused Thiazine-Dicarboxylates and Thiazole-Pyrimidines via One-Pot Three-Component Reactions." Molecules 26, no. 18 (2021): 5493. http://dx.doi.org/10.3390/molecules26185493.

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A facile and efficient one-pot three-component reaction method for the synthesis of thiazine-dicarboxylates is reported. Reaction of an isocyanide and dialkyl acetylenedicarboxylate with 2-amino-4H-1,3-thiazin-4-one derivatives containing both an acidic proton and an internal nucleophile gave the products in good yields of 76–85%. The reactivity of dialkyl acetylenedicarboxylates was further tested in the synthesis of thiazole-pyrimidines where a two-component reaction of 2-aminothiazole with dialkyl acetylenedicarboxylates was successfully converted to a more efficient three-component reactio

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Yennawar, Hemant P., Ryan Fox, and Lee J. Silverberg. "Crystal structure of the 1:1 adduct of 2,3-diphenyl-3,4,5,6-tetrahydro-2H-1,3-thiazin-4-one with triphenyltin chloride." Acta Crystallographica Section E Crystallographic Communications 72, no. 3 (2016): 276–79. http://dx.doi.org/10.1107/s2056989016001730.

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The title adduct, chlorido(2,3-diphenyl-3,4,5,6-tetrahydro-2H-1,3-thiazin-4-one-κO)triphenyltin, [Sn(C6H5)3Cl(C16H15NOS)], resulted from reaction of 2,3-diphenyl-3,4,5,6-tetrahydro-2H-1,3-thiazin-4-one with triphenyltin chloride. The thiazine ring has an envelope conformation with the S atom forming the flap. The molecule has five phenyl rings, two of them attached to the thiazine ring at positions 2 and 3, and three in coordination with the SnIVatom. The three rings of the triphenyltin group are involved in intramolecular interactions of different types, C—H...O, edge-to-face (or T-type) π–π

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Sharma, Anupama, Sarita Khaturia, and Har Lal Singh. "Synthesis of New Schiff Base of 1,3-Oxazine and 1,3-Thiazine Derivatives Derived from 4-Phenyl Substituted Chalcones and Evaluation of their Antibacterial Activity." Asian Journal of Chemistry 33, no. 3 (2021): 531–36. http://dx.doi.org/10.14233/ajchem.2021.23050.

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Oxazine and thiazine heterocycles have distinctive interests due to their important class of natural and non-natural products and exhibit high biological activities in the pharmaceutical and biological fields. This work was planned to synthesize Schiff base of 1,3-oxazine and 1,3-thiazine derivative from 4-phenyl substituted chalcones. The structures of the newly synthesized targeted compounds were established from UV, IR, 1H NMR, 13C NMR and DFT calculations. The molecular properties HOMO-LUMO energy, energy gap, softness and harness were calculated using DFT/B3LYP/6-311G (d,p) basis set. in

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Tuloup, Rémy, Renée Danion-Bougot, Daniel Danion, Jean-Paul Pradère, and Loïc Toupet. "Une application du cycle pyrazoline à la lactamisation et à la formylation de 6H thiazines-1,3." Canadian Journal of Chemistry 67, no. 7 (1989): 1125–31. http://dx.doi.org/10.1139/v89-169.

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A pyrazoline ring is used as a masking, a stereodirecting, and a latent formyl group in the synthesis of 7-amino-4-formyl cephems from 6H-1,3-thiazines. Keywords: thiazine, cephem, pyrazoline, benzeneseleninic anhydride.

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Dissertations / Theses on the topic "Thiazine"

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Sunwar, Chandra Bahadur. "Interaction of some thiazine dyes with clay minerals." Thesis, University of North Bengal, 1985. http://hdl.handle.net/123456789/847.

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Schneeweis, Arno [Verfasser], Thomas J. J. [Gutachter] Müller, and Klaus [Gutachter] Schaper. "Bis[1]benzothieno[1,4]thiazine - Der Weg zum antiaromatischen anellierten 1,4-Thiazin / Arno Schneeweis ; Gutachter: Thomas J.J. Müller, Klaus Schaper." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2019. http://d-nb.info/1188017470/34.

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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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Berens, Henning Robert Vinzenz [Verfasser], and Klaus [Gutachter] Schaper. "Disubstituierte Bis[1]benzothieno[1,4]thiazine und Di[1,4]thiophtheno[1,4]thiazine - Neue thiazinbasierte Heteropentacene mit erhöhter Elektronendichte / Henning Robert Vinzenz Berens ; Gutachter: Klaus Schaper." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2021. http://d-nb.info/1233007602/34.

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BENHADDA, DJAMILA. "Syntheses de thiazolines, thiazoles, thiazine-1, 3 ones-6 et thiazines-1, 3 a partir de n'-thioacylformamidines enethiolisables : application a la preparation de cephemes." Nantes, 1989. http://www.theses.fr/1989NANT2009.

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Loukou, Christina. "Thiazine-S-oxides as precursors to the synthesis of benzodiazepine and benzothiadiazepine heterocycles." Thesis, University of Huddersfield, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.399956.

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RONDEAU, DAVID. "Synthese et reduction electrochimique de 1,3-thiazine-6-ones et de thiopyranes actives." Rennes 1, 1997. http://www.theses.fr/1997REN10026.

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Ce travail est consacre a la synthese et a la reduction electrochimique, en milieu protique, d'heterocycles en serie 1,3-thiazine et thiopyrane. Les 1,3-thiazine-6-ones sont obtenues par reaction de cycloaddition entre une n-thioacylformamidine et un chlorure d'acide. L'etude du comportement electrochimique de ces composes met en evidence le role fondamental du substituant en position 4. Lorsque celui-ci est un groupement electroattracteur (r#4 = co#2et), la 1,3-thiazine-6-one subit, quel que soit le milieu, une reduction a 4 electrons avec regression cyclique : elimination de h#2s et formatio

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Bose, Himangshu Sekhar. "Metachromatic behaviour of some thiazine dyes in solution in presence of inorganic and organic electrolytes, surfactants, polyelectrolytes and clay minerals." Thesis, University of North Bengal, 1986. http://hdl.handle.net/123456789/731.

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Ducrey, Fiona. "Thiazines - 1,3 et céphèmes fonctionnalisés." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37597315m.

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LALANDE, AGNES. "Thiazides et tissu osseux." Paris 7, 1998. http://www.theses.fr/1998PA077239.

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Des etudes epidemiologiques ont montre que les diuretiques thiazidiques provoquent une diminution de la calciurie et entrainent ainsi une diminution la perte osseuse et du risque fracturaire. Dans un modele experimental de perte osseuse par supplementation en sodium chez des rats spontanement hypertendus, nous avons observe l'effet benefique de l'indapamide (idp), diuretique antihypertensif apparente aux thiazides, sur le tissu osseux. Chez ces rats shr supplementes en sodium, nous avons note que l'idp diminuait l'excretion urinaire du calcium. Par densitometrie et histomorphometrie, nous avon

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Books on the topic "Thiazine"

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International Conference on Phenothiazines and Structurally Related Psychotropic Compounds (6th 1990 Pasadena, Calif.). Thiazines and structurally related compounds: Proceedings of the Sixth International Conference on Phenothiazines and Structurally Related Psychotropic Compounds, Pasadena, California, September 11-14, 1990. Edited by Keyzer Hendrik and Eckert George M. Krieger Pub. Co., 1992.

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1926-, Richardson Robert G., ed. The Rheumatological disease process: Focus on piroxicam. Royal Society of Medicine, 1985.

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Svadlenka, Anton. Thiazole: Synthesis and Reactions. Nova Science Publishers, Incorporated, 2020.

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Thiazole: Synthesis and Reactions. Nova Science Publishers, Incorporated, 2020.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 3. Wiley & Sons, Incorporated, John, 2008.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2009.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2008.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 2. Wiley & Sons, Incorporated, John, 2009.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 2. Wiley & Sons, Limited, John, 2007.

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Thiazole and Its Derivatives, Part 3. Wiley & Sons, Incorporated, John, 2009.

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Book chapters on the topic "Thiazine"

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Van Thien, Tran. "Thiazine, Oxazine, and Phenazine Leuco Dyes." In Chemistry and Applications of Leuco Dyes. Springer US, 2002. http://dx.doi.org/10.1007/0-306-46906-5_3.

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Xu, Zhengshuang, and Tao Ye. "Thiazoline and Thiazole and their Derivatives." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch13.

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Peter, Helga. "Thiazide." In Springer Reference Medizin. Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/978-3-642-54672-3_822-1.

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Peter, Helga. "Thiazide." In Springer Reference Medizin. Springer Berlin Heidelberg, 2025. https://doi.org/10.1007/978-3-662-65186-5_822.

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Pragathi, Mederametla, and Palanisamy Suresh Babu. "Erythrosine dye decolorization by sonolysis and its performance evaluation under varying pH conditions of thiazine dye." In Applications of Mathematics in Science and Technology. CRC Press, 2025. https://doi.org/10.1201/9781003606659-88.

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Velázquez, H., H. Knauf, and E. Mutscler. "Thiazide Diuretics." In Diuretics. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-79565-7_8.

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Cioffi, William G., Michael D. Connolly, Charles A. Adams, et al. "Thiazide Diuretics." In Encyclopedia of Intensive Care Medicine. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-00418-6_2285.

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Pansare, Dattatraya, Mubarak H. Shaikh, Pravin Chavan, et al. "Synthesis and Biological Evaluation of Thiazoline, Thiophene and Thiazole Scaffolds." In S-Heterocycles. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-4308-7_3.

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Wilson, John Fawcett. "Thiazides." In The Immunoassay Kit Directory. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0679-5_50.

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Pragathi, Mederametla, and Palanisamy Suresh Babu. "Investigation and Assessment of the Degrading Potential of Hazardous Brilliant Blue Dye using Sonolysis and its Efficacy Against Thiazine Dye." In Case Studies on Holistic Medical Interventions. CRC Press, 2024. https://doi.org/10.1201/9781003596684-141.

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Conference papers on the topic "Thiazine"

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Shuchi, Nuren, Tyler Adams, V. Paige Stinson, et al. "Complex Dielectric Function of Photochromic Thiazolothiazole Embedded Polymers Determined by Spectroscopic Ellipsometry." In CLEO: Applications and Technology. Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_at.2024.jth2a.10.

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The complex dielectric function of photochromic thiazolo[5,4-d]thiazole embedded in polymer is reported in the spectral range from 0.8 to 2.5 eV. Strong absorption bands in the measured spectral range are observed depending upon its redox states.

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Cheng, Jianqun, Ke Chen, Yan Wang, and Mingju Huang. "Comparison of high-density holographic characteristics of photopolymers sensitized by two kinds of thiazine dyes." In Eighth International Symposium on Optical Storage and 2008 International Workshop on Information Data Storage, edited by Fuxi Gan. SPIE, 2008. http://dx.doi.org/10.1117/12.822045.

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Pragathi, Mederametla, and Palanisamy Suresh Babu. "Performance evaluation of decolorizing tartrazine dye under standard conditions using sonolysis against thiazine dye in varying pH and temperature." In 2ND INTERNATIONAL INTERDISCIPLINARY SCIENTIFIC CONFERENCE ON GREEN ENERGY, ENVIRONMENTAL AND RENEWABLE ENERGY, ADVANCED MATERIALS, AND SUSTAINABLE DEVELOPMENT: ICGRMSD24. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0238404.

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Pragathi, Mederametla, and Palanisamy Suresh Babu. "Performance evaluation of decolorizing tartrazine dye under standard conditions using sonolysis against thiazine dye in varying pH and temperature." In INNOVATIONS IN THERMAL, MANUFACTURING, STRUCTURAL AND ENVIRONMENTAL ENGINEERING: ICITMSEE’24. AIP Publishing, 2025. https://doi.org/10.1063/5.0264640.

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Gamba, Gerardo, Daniela Riccardi, James C. Williams, Andrew P. Evan, James E. Lingeman, and James A. McAteer. "Cell Biology of Thiazide Bone Effects." In RENAL STONE DISEASE 2: 2nd International Urolithiasis Research Symposium. AIP, 2008. http://dx.doi.org/10.1063/1.2998060.

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Falabella, Petra, and Željka Večerić-Haler. "Arginine Vasopressin Resistance (AVP-R)." In Socratic Lectures 11. University of Lubljana Press, 2024. http://dx.doi.org/10.55295/psl.11.2024.1.

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Arginine vasopressin resistance (AVP-R) previously known as nephrogenic diabetes insipidus is a rare disorder characterised with large fluid output due to resistance to arginine vasopressin in kidneys. It can be caused by different etiologies, including hereditary causes. In diagnosis we must determine the reason for polyuria (vasopressin deficiency, resistance, or primary polydipsia). Treatment is mostly symptomatic with adequate water consumption in combination with low-salt and low-protein diet. The main drugs used to treat AVP-R are thiazide diuretics, non-steroidal anti-inflammatory drugs

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Miloradović, Vladimir, and Neda Ćićarić. "Approaches in the Treatment of Uncontrolled Hypertension." In 7th International Congress of Cardionephrology KARNEF 2025. Punta Niš, 2025. https://doi.org/10.46793/karnef25.332m.

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Despite the availability of antihypertensive drugs, many patients worldwide have uncontrolled hypertension (1,2). In this regard, the term „resistant hypertension“ was introduced, with a prevalence of 10%-20% in hypertensive patients (3). According to the current guidelines of the European Association of Cardiology, hypertension is defined as resistant when the treatment strategy, which includes appropriate lifestyle measures and treatment with maximum or maximally tolerated doses of diuretics (thiazides and thiazide-like diuretics), blockers of the renin-angiotension-aldosterone system (RAAS)

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Ghodgaonkar, Sunayana, Jinish Shah, Sachin Laddha, Sandeep Waghulde, and Vaibhav Kulkarni. "Synthesis and Evaluation of Novel Thiazole Derivatives." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00397.

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Schneider, Juliana M. F. M., Paulo H. Schneider, and Aloir A. Merlo. "2-Thiazoline Amide Derivatives as Liquid Crystals." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0051-1.

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Imberty, Anne, Jean-Paul Pradére, Michel Jubault, and André Tallec. "Molecular orbital calculations and electroreduction selectivity of 1,3-thiazines and thiazinones." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47676.

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