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Relevant bibliographies by topics / ] thiadiazine derivatives

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Academic literature on the topic '] thiadiazine derivatives'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "] thiadiazine derivatives"

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Innes, Dylan, Michael V. Perkins, Andris J. Liepa, and Craig L. Francis. "N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. Part XIV. Synthesis and Reactivity of the New Benzo[4,5]imidazo[1,2-b][1,2,6]thiadiazine Ring System." Australian Journal of Chemistry 71, no. 1 (2018): 58. http://dx.doi.org/10.1071/ch17255.

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N,N-Dialkyl-N′-chlorosulfonyl chloroformamidines 1 underwent regioselective reactions with the 1,3-NCC bis-nucleophilic 1H-benzimidazole-2-acetonitriles 4 and related compounds to produce benzo[4,5]imidazo[1,2-b][1,2,6]thiadiazine dioxides 6, 9, 12, and 14, representatives of a new ring system. Reaction of dichlorides 1 with trifluoroacetyl derivative 16 afforded benzo[4,5]imidazo[1,2-c]pyrimidines 19 and 20. An N-acyl and some N-alkyl derivatives of benzimidazo-thiadiazines 6 were prepared to demonstrate the potential of this new ring system as a novel scaffold for synthetic and medicinal che

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Mostafa, Mohamed S., Ibrahim Ali M. Radini, Naglaa M. Abd El-Rahman, and Rizk E. Khidre. "Synthetic Methods and Pharmacological Potentials of Triazolothiadiazines: A Review." Molecules 29, no. 6 (2024): 1326. http://dx.doi.org/10.3390/molecules29061326.

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This review article examines the synthetic pathways for triazolothiadiazine derivatives, such as triazolo[3,4-b]thiadiazines, triazolo[5,1-b]thiadiazines, and triazolo[4,3-c]thiadiazines, originating from triazole derivatives, thiadiazine derivatives, or thiocarbohydrazide. The triazolothiadiazine derivatives exhibit several biological actions, including antibacterial, anticancer, antiviral, antiproliferative, analgesic, anti-inflammatory, and antioxidant properties. The review article aims to assist researchers in creating new biologically active compounds for designing target-oriented triazo

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Mlostoń, Grzegorz, Katarzyna Urbaniak, Malwina Sobiecka, et al. "Hetero-Diels-Alder Reactions of In Situ-Generated Azoalkenes with Thioketones; Experimental and Theoretical Studies." Molecules 26, no. 9 (2021): 2544. http://dx.doi.org/10.3390/molecules26092544.

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The hetero-Diels-Alder reactions of in situ-generated azoalkenes with thioketones were shown to offer a straightforward method for an efficient and regioselective synthesis of scarcely known N-substituted 1,3,4-thiadiazine derivatives. The scope of the method was fairly broad, allowing the use of a series of aryl-, ferrocenyl-, and alkyl-substituted thioketones. However, in the case of N-tosyl-substituted cycloadducts derived from 1-thioxo-2,2,4,4-tetramethylcyclobutan-3-one and the structurally analogous 1,3-dithione, a more complicated pathway was observed. By elimination of toluene sulfinic

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Yan, Jinghua, Weijie Si, Haoran Hu, Xu Zhao, Min Chen, and Xiaobin Wang. "Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group." PeerJ 7 (September 6, 2019): e7581. http://dx.doi.org/10.7717/peerj.7581.

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A series of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group was designed and synthesized. The structures of all the compounds were well characterized using 1H NMR, 13C NMR and high-resolution mass spectrometer, and further confirmed by the X-ray diffraction analysis of 8d. The antimicrobial activities of all the target compounds against Xanthomonas oryzae pv. oryzicola, X. oryzae pv. oryzae, Rhizoctonia solani and Fusarium graminearum were evaluated. The in vitro antimicrobial bioassays indicated that some title compounds exhibited noteworthy antimicrobial eff

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El-Sayed, Wael A., Omar M. Ali, Marwa M. Hathoot, and Adel A. H. Abdel-Rahman. "Synthesis and Antimicrobial Activity of New Substituted Fused 1,2,4-Triazole Derivatives." Zeitschrift für Naturforschung C 65, no. 1-2 (2010): 22–28. http://dx.doi.org/10.1515/znc-2010-1-204.

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A number of new substituted 1,2,4-triazole, 1,2,4-triazolo[3,4-b]1,3,4-thiadiazole and 1,2,4-triazolo[3,4-b]1,3,4-thiadiazine derivatives were synthesized and tested for their antimicrobial activity against Bacillus subtilis (Gram-positive), Pseudomonas aeruginosa (Gramnegative), and Streptomyces species (Actinomycetes). The synthesized compounds displayed different degrees of antimicrobial activities or inhibitory actions.

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Gong, Tang, Liu та Liu. "Synthesis and Evaluation of Novel 2H-Benzo[e]-[1,2,4]thiadiazine 1,1-Dioxide Derivatives as PI3Kδ Inhibitors". Molecules 24, № 23 (2019): 4299. http://dx.doi.org/10.3390/molecules24234299.

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In previous work, we applied the rotation-limiting strategy and introduced a substituent at the 3-position of the pyrazolo [3,4-d]pyrimidin-4-amine as the affinity element to interact with the deeper hydrophobic pocket, discovered a series of novel quinazolinones as potent PI3Kδ inhibitors. Among them, the indole derivative 3 is one of the most selective PI3Kδ inhibitors and the 3,4-dimethoxyphenyl derivative 4 is a potent and selective dual PI3Kδ/γ inhibitor. In this study, we replaced the carbonyl group in the quinazolinone core with a sulfonyl group, designed a series of novel 2H-benzo[e][1

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Alsahib, Sanaa abdul. "Characterization and Biological Activity of Some New Derivatives Derived from Sulfamethoxazole Compound." Baghdad Science Journal 17, no. 2 (2020): 0471. http://dx.doi.org/10.21123/bsj.2020.17.2.0471.

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A new series of Sulfamethoxazole derivatives was prepared and examined for antifibrinolytic and antimicrobial activities. Sulfamethoxazole derivatives bear heterocyclic moieties such as 1,3,4-thiadiazine {3}, pyrazolidine-3,5-diol {4} 6-hydroxy-1,3,4-thiadiazinane-2-thione {5} and [(3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-yl)diazenyl] {8}. Their structures were elucidated by spectral methods (FT-IR, H1-NMR). Physical properties are also determined for all compound derivatives. Recently prepared compounds were tested for their antimicrobial activity in the laboratory. Each screened compound sho

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Abu-Hashem, Ameen Ali, and Rasha A. M. Faty. "Synthesis, Antimicrobial Evaluation of Some New 1, 3, 4-Thiadiazoles and 1, 3, 4- Thiadiazines." Current Organic Synthesis 15, no. 8 (2018): 1161–70. http://dx.doi.org/10.2174/1570179415666180720114547.

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Background: 1, 3, 4-thiadiazoles, 1, 3, 4-thiadiazines and thienopyrimidines have newly attracted attention due to their forceful pharmacological activities. They showed antimicrobial, antiviral, analgesic and anti-inflammatory properties. Objective: The aim of this research is to synthesize new thiadiazolothienopyrimidines (2-10), thienopyrimidothiadiazines (11-15), quinoxaline-thienopyrimidinones (16) and thienopyrimido- thiadiazinoquinoxalinones (17) via effectual high yield procedure for assessing their antimicrobial activity. Method: A series of new 1, 3, 4-thiadiazolothienopyrimidines, t

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Naqui, Jahan Siddiqui* Atul Barsagade Mohammad Idrees. "SYNTHESIS, ANTIMICROBIAL AND ANTIOXIDANT ACTIVITIES OF 1,3,5-THIADIAZINE DERIVATIVES." Indo American Journal of Pharmaceutical Sciences 04, no. 10 (2017): 3655–63. https://doi.org/10.5281/zenodo.1035798.

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A series of N-(4-(benzyloxy)benzylidene)-2-(arylimino)-6-(phenylimino)-3,6-dihydro-2H-1,3,5-thiadiazin-4- amine derivatives (4a-d) have been synthesized by condensation of 1-(N-4-(benzyloxy) benzylidenecarbamimidoyl)-3-arylthiourea (3a-d) with phenyl isocyanodichloride. Interaction of 1- carbamimidoyl-3-arylthiourea (2a-d) and p-benzyloxy benzaldehyde yielded (3a-d). Monoacetyl (5b) and mononitroso (6b) derivatives were also synthesised by substitution of hydrogen atom of cyclic –NH- of 4b on treatment with acetic anhydride and sodium nitrite respectively. Further, 4b upon boiling with 5% aque

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Obydennov, Konstantin L'vovich, Tatiana Andreevna Kalinina, Olga Alexandrovna Vysokova, et al. "The different modes of chiral [1,2,3]triazolo[5,1-b][1,3,4]thiadiazines: crystal packing, conformation investigation and cellular activity." Acta Crystallographica Section C Structural Chemistry 76, no. 8 (2020): 795–809. http://dx.doi.org/10.1107/s2053229620009328.

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The crystal structures of four new chiral [1,2,3]triazolo[5,1-b][1,3,4]thiadiazines are described, namely, ethyl 5′-benzoyl-5′H,7′H-spiro[cyclohexane-1,6′-[1,2,3]triazolo[5,1-b][1,3,4]thiadiazine]-3′-carboxylate, C19H22N4O3S, ethyl 5′-(4-methoxybenzoyl)-5′H,7′H-spiro[cyclohexane-1,6′-[1,2,3]triazolo[5,1-b][1,3,4]thiadiazine]-3′-carboxylate, C20H24N4O4S, ethyl 6,6-dimethyl-5-(4-methylbenzoyl)-6,7-dihydro-5H-[1,2,3]triazolo[5,1-b][1,3,4]thiadiazine-3-carboxylate, C17H20N4O3S, and ethyl 5-benzoyl-6-(4-methoxyphenyl)-6,7-dihydro-5H-[1,2,3]triazolo[5,1-b][1,3,4]thiadiazine-3-carboxylate, C21H20N4O4

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Dissertations / Theses on the topic "] thiadiazine derivatives"

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LI, PETRI Giovanna. "SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW IMIDAZO[2,1-b][1,3,4]THIADIAZOLE DERIVATIVES AS ANTICANCER AND ANTIBIOFILM AGENTS, AND PRECLINICAL INVESTIGATION OF ANTI-LDH-A COMPOUNDS AGAINST MALIGNANT MESOTHELIOMA." Doctoral thesis, Università degli Studi di Palermo, 2020. http://hdl.handle.net/10447/395253.

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SCIANO', Fabio. "Development of natural and synthetic compounds as kinase inhibitors targeting cancer cells and cancer stem cells." Doctoral thesis, Università degli Studi di Palermo, 2023. https://hdl.handle.net/10447/580156.

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Picart, Sébastien. "Fonctionnalisation de la polyaniline par des composés soufrés électroactifs en vue de son utilisation en batteries au lithium." Université Joseph Fourier (Grenoble), 1995. http://www.theses.fr/1995GRE10236.

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Ce travail se situe dans le cadre de l'application des polymeres conducteurs electroniques (pce) aux batteries rechargeables. L'objectif a ete d'associer deux partenaires aux proprietes electrochimiques complementaires: un pce, la polyaniline, connue pour sa bonne tenue a la charge permanente, une autodecharge faible et une cyclabilite elevee en batterie, et un systeme electroactif base sur le couple redox disulfure/dithiolate qui presente une forte densite d'energie massique. Trois voies ont ete successivement explorees: - la preparation d'une polyaniline substituee sur le cycle par un groupe

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廖培因. "Design and Synthesis of 6-oxo-indolo[1,2-b]benzo[1,2,4]thiadiazine 12,12-dioxide Derivatives as Potential Anticancer Agents." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/42443269891015872005.

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碩士<br>國立臺灣大學<br>藥學研究所<br>90<br>This thesis is aimed in (i) the design and synthesis of 6-oxo-indolo[1,2-b]benzo[1,2,4]thiadiazine 12,12-dioxide derivatives, analogues of tryptanthrin, as potential novel anticancer drugs; (ii) tryptanthrin containing polyamine side chain, by enhancing the binding ability with DNA to act as stabilizing agent of triplex DNA. Due to the results of satisfactory inhibitory activities of tryptanthrin derivatives against various cancer cell lines, 6-oxo-indolo[1,2-b]benzo[1,2,4]thiadiazine 12,12-dioxide (23) and its derivatives were designed and synthesized on the ba

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Jia, Huang Shing, and 黃信嘉. "Synthesis and Characteristics of 1,3,4-Thiadiazole Derivatives." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/12191180337143130451.

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碩士<br>國立臺灣科技大學<br>高分子工程系<br>92<br>The investigation was prepared by the reaction with thiosemicarbazide, carbon disulfide, p-substiuented-benzoic acid in ethanol at refluxed to get 1,3,4-thiadiazole(3、5a~5d). Then 1,3,4-thiadiazole derivatives coupled with N-substiuented-pyridone derivatives(12a~12j) and pyroazolone derivatives(13a~13j). Furthermore, 1,3,4-thiadiazole intermediates were reacted with cyanuric chloride to give a reactive dyes (20), and these dyes condensed with hydrazine hydrate and 4-nitrobenzaldehyde in ethanol to obtain azo-methine dyes (26a~26b)。 Characterization

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Fan, Chun-Yi, and 范俊義. "Synthesis and characteristics of 2-amino-1,3,4-thiadiazole derivatives." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/18583447828238608043.

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碩士<br>國立中央大學<br>化學工程與材料工程研究所<br>93<br>A series of 2-Amino-1,3,4-thiodazole has been synthesized which exhibit various yields of 32~94%. The reaction conditions were that thio- semicarbazide: (1) and aromatic(or heterocyclic)acid were put into Phosphorus oxy- chloride (POCl3), then were heated and refluxed, seven kinds of Ⅰa ~ Ⅰe, Ⅱa~Ⅱb can be obtained. (2) reacted with isonicotinic acid and cyclodehydration by Poly- phosphoric acid (PPA). 2-amino-5-(4-pyridyl)-1,3,4-thiadiazole(Ⅰf) was obtained. (3) reacted with formic acid in concentrated hydrochloride, 2-amino- 1,3,4-thiadiazole(Ⅰg) can be o

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吳乃群. "Studies on carbonic anhydrase inhibitors:physicochemical properties and bioactivity of Thiadiazole Derivatives." Thesis, 1991. http://ndltd.ncl.edu.tw/handle/97692256917437620609.

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Huang, Cheng-Huan, and 黃承驩. "Design and Synthesis of Benzo[c][1,2,5]thiadiazole derivatives as TADF Emitters." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/jbtzbg.

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碩士<br>國立中山大學<br>光電工程學系研究所<br>106<br>In this study, a new blue Thermally Activated Delayed Fluorescence (TADF) , we call it ” BTZ-PXZ ” is designed and synthesized. The ΔEST of 4,7-di(10H- phenoxazin-10-yl)benzo[c][1,2,5]thiadiazole (BTZ-PXZ) is lower than 4,7-bis(9H- carbazol-9-yl)benzo[c][1,2,5]thiadiazole (BTZ-CZ), 4,7-bis(9,9-dimethylacridin- 10(9H)-yl)benzo[c][1,2,5]thiadiazole (BTZ-DMAZ) and N4,N4,N7,N7-tetraphenyl- benzo[c][1,2,5]thiadiazole-4,7-diamine (BTZ-DPA) which we can find some related papers in Journal of Materials Chemistry C. In this way, BTZ-PXZ can reduce the effect of singl

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LING, WU CHENG, and 巫政霖. "Studies on the Syntheses and Pharmacological Properties of Indole﹑Thiadiazole and Thiazoline Derivatives." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/80257222282047794315.

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Huang, Chih-wei, and 黃致瑋. "Novel Isomers of Organic Mesogens Derived from Two Different Isomeric Biphenol Derivatives and New Organic Mesogens Derived from 1,3,4-oxadiazole or 1,3,4- thiadiazole Derivatives." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/63609626498491425298.

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碩士<br>國立中央大學<br>化學研究所<br>100<br>Part I A new type of 3,3’-biphenol/4,4’-biphenol isomer derivatives exhibiting mesomorphic properties were synthesized and their mesomorphic properties examined. All compounds were characterized by 1H and 13C-NMR spectroscopy. Their mesomorphic properties were studied by differential scanning calorimetry (DSC), polarized optical microscopy (POM) and powder x-ray diffraction (XRD). These molecules have two ester linkages (1a, 1b, 2a, 2b), two (1c, 1e, 2c, 2e), and four alkoxy sidechains (1d, 1f, 2d, 2f). The compounds have been synthesized by Schiff base from 1a

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Book chapters on the topic "] thiadiazine derivatives"

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Kabi, Arup K., Raghuram Gujjarappa, Aakriti Garg, et al. "Highlights on Biological Activities of 1,3,4-Thiadiazole and Indazole Derivatives." In Tailored Functional Materials. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-2572-6_7.

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Desai, Kishor R., and Bhavin R. Patel. "Various Synthetic Strategies and Therapeutic Potential of Thiadiazole, Oxadiazole, Isoxazole and Isothiazole Derivatives." In N-Heterocycles. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_6.

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Varvaresou, Athanasia, Anna Tsantili-Kakoulidou, and Theodora Siatra-Papastaikoudi. "A Critical Appraisal of logP Calculation Procedures Using Experimental Octanol-Water and Cyclohexane-Water Partition Coefficients and HPLC Capacity Factors for a Series of Indole Containing Derivatives of 1,3,4-Thiadiazole and 1,2,4-Triazole." In Molecular Modeling and Prediction of Bioactivity. Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4141-7_133.

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Nagendra, G., D. N. Akshitha, H. S. Lalithamba, and G. K. Prashanth. "Thiadiazoles." In Advances in Chemical and Materials Engineering. IGI Global, 2025. https://doi.org/10.4018/979-8-3693-7267-8.ch013.

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Heterocycles containing nitrogen, oxygen and sulfur have been under investigation for a long time because of their important medicinal properties. The literature survey has described that thiadiazole moieties serve as analgesic, anti-inflammatory, anti-microbial activities, antihypertensive,anticancer, antituberculosis and vasodilator and this heterocyclic nucleus still possess considerable characteristics to attract the chemists for designing of newer biologically active molecules. Among them 1,2,4-thiadiazole, 1,3,4-thiadiazole and their derivatives are recognized as heterocyclic nuclei of g

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Mohite, Popat, Nitin Bhoge, Sujata G. Dengale, and Nirmala R. Darekar. "Synthesis, Properties, and Biological Applications of 1,2,4-Thiadiazoles." In S-Heterocycles. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/9781837674015-00133.

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This chapter provides a comprehensive overview of recent advances in the preparation and biological applications of 1,2,4-thiadiazole, a versatile heterocyclic compound with diverse pharmacological properties. This chapter begins with the exploration of various synthetic strategies, ranging from traditional methods to sustainable and green approaches, highlighting their impact on synthetic efficiency and environmental considerations. The focus is then shifted to the biological applications of 1,2,4-thiadiazole derivatives, which show pharmacological activities, such as antioxidant, antimicrobi

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Palekar, Vikrant Sudhakar, and Kulbhushan A. Sasane. "Examining Biological Relevence of Thiazolo Thiadiazole and Thiazolo Thiazole Fused Heterocyles." In Advances in Bioinformatics and Biomedical Engineering. IGI Global, 2024. http://dx.doi.org/10.4018/979-8-3693-7520-4.ch005.

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Aromatic Fused heterocycles containing Nitrogen (N) and Sulfur(S) has extraordinary bioactive behavior due to which they are attracting the interest of chemists worldwide & thus used as a potential material in medicinal/pharmaceutical industries. The nitrogen-sulphur fused heterocycles attracting attention of the researchers due to number of biological and pharmacological activities and observed to exhibit extensive applications in drug discovery and development. The efforts are made to understand biological activity based on position of heteroatom & the substituent present in 5-member

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Cailler, Lucie P., Alexander G. Martynov, Yulia G. Gorbunova, Aslan Yu Tsivadze, and Alexander B. Sorokin. "Carbene insertion to N–H bonds of 2-aminothiazole and 2-amino-1,3,4-thiadiazole derivatives catalyzed by iron phthalocyanine." In Porphyrin Science by Women. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811223556_0106.

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Conference papers on the topic "] thiadiazine derivatives"

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Nekrasa, Ivan, Elena Bibik, and Sergey Krivokolysko. "Antidepressive Activity of a Series of Tetrahydropyrido[2,1-B][1,3,5]thiadiazine Derivatives in Forced Swimming Test by Porsolt." In 3rd International Electronic Conference on Medicinal Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecmc-3-04703.

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Nekrasa, Ivan, Helen Bibik, Sergey Krivokolysko, Viktor Dotsenko, Konstantin Frolov, and Aliona Startseva. "Evaluation of the impact of tetrahydropyrido[2,1-b][1,3,5]thiadiazine derivatives on lepodova effects in the test of suspension by the tail." In 5th International Electronic Conference on Medicinal Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06295.

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Marquez-Lucero, Alfredo. "Thiadiazole derivatives with nonlinear optical properties." In Integrated Optoelectronic Devices 2005, edited by James G. Grote, Toshikuni Kaino, and Francois Kajzar. SPIE, 2005. http://dx.doi.org/10.1117/12.582050.

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Dimić, Dušan, Dejan Milenković, Edina Avdović, Goran Kaluđerović, and Jasmina Dimitrić Marković. "MOLECULAR DOCKING AND MOLECULAR DYNAMICS STUDIES OF THE INTERACTION BETWEEN COUMARIN-NEUROTRANSMITTER DERIVATIVES AND CARBONIC ANHYDRASE IX." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.056d.

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Novel biologically active compounds can be obtained by the structural modification of coumarins. In this contribution, five new derivatives of 4-hydroxycoumarin with tyramine, octopamine, norepinephrine, 3-methoxytyramine, and dopamine were obtained. Their structures were optimized based on the previously obtained crystal structure of the 4-hydroxycoumarin-dopamine derivative. The special emphasis was put on the effect of various substituents on the structure of obtained compounds and intramolecular interactions governing the stability. To investigate their possible antitumor activity, molecul

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Tiuleanu, Pavel, Ivan Marenin, and Andrei Shchekotikhin. "Synthesis and evaluation of new 2-azolylindoles - derivatives of indole-2-carboxylic." In Conferința științifică națională cu participare internațională "Integrare prin cercetare și inovare", dedicată Zilei Internaționale a Științei pentru Pace și Dezvoltare. Moldova State University, 2025. https://doi.org/10.59295/spd2024n.91.

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Indole-2-carboxylic acid is a promising scaffold for the design of new compounds with application in biological studies and medicine practice. Its derivatives have shown a wide range of biological activity: antiviral, antifungal, antibacterial, anti-inflammatory. As part of the presented study, the method for preparation of alkyl derivatives of acetoacetic ester has been optimized. These derivatives are intermediates for the synthesis of indole-2-carboxylic acid esters according to the Japp-Klingemann/Fisher methodology. Several methods for the transformation of indole-2-carboxylic acid ester

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Ananda, S., V. Keerthikumara, H. Kumar Keshav, et al. "Structural, DFT and nonlinear optical studies of hemihydrate thiadiazole derivative." In 66TH DAE SOLID STATE PHYSICS SYMPOSIUM. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0178379.

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"Efficient Synthesis of Conjugated 1,3,4-Thiadiazole Derivatives under Suzuki Cross-Coupling Reactions." In 2023 4th International Scientific Conference "Chemical Technology and Engineering". Lviv Polytechnic National University, 2023. http://dx.doi.org/10.23939/cte2023.182.

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Ayyash, Ahmed Neamah. "A new [1,2,4] triazolo [3,4-B] [1,3,4] thiadiazepine derivatives: Synthesis and antimicrobial studies." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0027404.

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Qiu, Yong, and Ruiping Gao. "Ambipolar Transporting Naphtho[2,3-c][1,2,5]thiadiazole Derivatives for Non-Doped Red-Emitting OLEDs." In Organic Materials and Devices for Displays and Energy Conversion. OSA, 2007. http://dx.doi.org/10.1364/omd.2007.otud5.

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Zhu, Fangkun, Wenxiu Fan, Li Qu, and Hailing Hao. "Prepation and tribological investigation of a novel S-N style 1,3,4-thiadiazole-2-thione derivatives." In 2011 International Conference on Consumer Electronics, Communications and Networks (CECNet). IEEE, 2011. http://dx.doi.org/10.1109/cecnet.2011.5768657.

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