Academic literature on the topic 'Thiocoumarines'

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Journal articles on the topic "Thiocoumarines"

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El-Ahmad, Youssef, and Pierre Reynaud. "Sur le mécanisme de la réaction de meth-cohn-tarnowski de préparation des thiocoumarines." Journal of Heterocyclic Chemistry 25, no. 3 (1988): 711–14. http://dx.doi.org/10.1002/jhet.5570250302.

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2

Mokrov, G. V., S. A. Litvinova, T. A. Voronina, et al. "Design, synthesis, and anticonvulsant evaluation of 4-GABA-3-nitrocoumarines, 1-thiocoumarines, quinolone-2-ones, and their derivatives." Medicinal Chemistry Research 28, no. 11 (2019): 1901–11. http://dx.doi.org/10.1007/s00044-019-02422-5.

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Chaudhary, Diksha, Tanay Pramanik, and Soumava Santra. "Thiocoumarins and Dithiocoumarins: Advances in Synthesis and Pharmacological Activity." Current Organic Chemistry 24, no. 16 (2020): 1793–814. http://dx.doi.org/10.2174/1385272824999200812132707.

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Thiocoumarins and dithiocoumarins are two important classes of sulphurcontaining heterocyclic compounds, which are bioisosteres of coumarins. Herein, various synthetic strategies for these two classes of heterocyclic compounds reported in the literature have been discussed. Different solvents, catalysts, reagents and reaction conditions, which were employed successfully for synthesizing thiocoumarins and dithiocoumarins have also been described concisely in this review. Mechanistic overview has been given wherever it was necessary. In addition, a comparative view of various solvents, catalysts
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Tiwari, Monika R., and Navin B. Patel. "Synthesis and Pharmacological Activities of Oxadiazole and Pyrimidine Bearing Thiocoumarin Derivatives." Current Microwave Chemistry 8, no. 1 (2021): 33–43. http://dx.doi.org/10.2174/2213335608666210401152153.

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Aims: The study aims to synthesize thiocoumarin scaffolds clubbed with pyrimidine and 1,3,4-oxadiazole ring system under microwave irradiation and describe their pharmacological activities. Background: We report herein an efficient and simple Lewis acid-catalyzed procedure for the synthesis of novel series of thiocoumarin clubbed with pyrimidine and 1,3,4-oxadiazole motifs under microwave irradiation. The microwave-assisted technique has many advantages, such as a higher yield, a clean and selective procedure, shorter reaction time, and simple work-up. Objective: The objective of the present s
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Balde, L., N. Rodier, Y. Elahmad, and P. Reynaud. "N-Diméthylaminoéthylcarboxamido-3 imino-2 thiocoumarine." Acta Crystallographica Section C Crystal Structure Communications 43, no. 8 (1987): 1592–94. http://dx.doi.org/10.1107/s0108270187090966.

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Karbe, Carolin, and Paul Margaretha. "Photocycloadditions to 1-thiocoumarin." Journal of Photochemistry and Photobiology A: Chemistry 57, no. 1-3 (1991): 231–33. http://dx.doi.org/10.1016/1010-6030(91)85018-c.

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Debnath, Mintu, Supriya Sasmal та Debasish Haldar. "Fabrication of egg shell-like nanovesicles from a thiocoumarin-based ε-amino ester: a potential carrier". Journal of Materials Chemistry B 5, № 27 (2017): 5450–57. http://dx.doi.org/10.1039/c7tb00025a.

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Arumugam, S., and C. L. Khetrapal. "Nuclear magnetic resonance spectra of oriented bicyclic systems containing heteroatom(s): the spectrum of 2-thiocoumarin." Canadian Journal of Chemistry 64, no. 4 (1986): 714–16. http://dx.doi.org/10.1139/v86-114.

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From the proton nmr studies of 2-thiocoumarin and coumarin, it is concluded that the relative interproton distances in the two oxygen heteroatom bicyclic systems are similar. The values for the phenyl ring protons do not deviate significantly from the regular hexagonal geometry, unlike bicyclic systems with nitrogens as the heteroatoms, such as diazanaphthalenes. Larger values of the indirect spin–spin couplings within the protons of the ring containing the oxygen heteroatom, compared to the values between the ortho protons in the phenyl rings in coumarin and 2-thiocoumarin, correspond to the
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Smith, David G., Linda Mitchell, and Elizabeth J. New. "Pattern recognition of toxic metal ions using a single-probe thiocoumarin array." Analyst 144, no. 1 (2019): 230–36. http://dx.doi.org/10.1039/c8an01747f.

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Zaitceva, Olesia, Valérie Bénéteau, Dmitry S. Ryabukhin, Benoit Louis, Aleksander V. Vasilyev, and Patrick Pale. "Zeolite‐promoted Synthesis of Coumarins and Thiocoumarins." ChemCatChem 12, no. 1 (2019): 326–33. http://dx.doi.org/10.1002/cctc.201901384.

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Dissertations / Theses on the topic "Thiocoumarines"

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Zaitceva, Olesia. "Development of new synthetic tools for the preparation of coumarins and thiocoumarins." Thesis, Strasbourg, 2019. http://www.theses.fr/2019STRAF014.

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Pour la première fois la coumarine a été isolée à l’état naturel en 1820. Depuis, les scientifiques ont extraits plus d’une mille de combinaisons de coumarines et développé plusieurs voies de leur synthèses. Les coumarines sont largement utilisées en pharmacie, médecine, chimie optique et biochimie. Thiocoumarine quant à elle intervient dans les domaines similaires à celui de coumarine. Grâce à ce vaste champ d’applications de coumarines et un grand potentiel de thiocoumarines, nous avons décidé de mettre au point de nouvelles méthodes pour synthétiser ces composants. Le but principal de notre
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Xu, Zhanjie. "Nouvelle synthèse de dérivés hétérocycliques thiazoliques, sélénazoliques, coumariniques, thiocoumariniques et quinolonéiques. Étude et évaluation de leur activité potentielle anticancéreuse." Thesis, Université de Lorraine, 2014. http://www.theses.fr/2014LORR0079/document.

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Nous avons réalisé la synthèse de thiazoles, sélénazoles, thiéno[2,3-d]thiazoles et thiéno[2,3-d][1,3]sélénazoles, ce dernier étant préparé facilement à partir de cyanamide et de sulfure de carbone. Nous avons de cette manière pu synthétiser des 4-amino-1,3-thiazoles et 1,3-sélénazoles substitués en position 2 et 5 en deux étapes. Appliqué ces hétérocycles, les 4-halogéno-1,3-thiazoles et 1,3-sélénazoles ont été synthétisés par la méthode de Doyle. La labilité des halogènes dans les dérivés précédents a permis de préparer de nouveaux thiéno[2,3-d]thiazoles et [1,3]sélénazoles. La détermination
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