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Relevant bibliographies by topics / Benzothiazol

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Academic literature on the topic 'Benzothiazol'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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Journal articles on the topic "Benzothiazol"

1

Višņevska, J., E. Jaščenko, I. Šestakova, A. Gulbe, and E. Ābele. "Unusual Synthesis and Cytotoxicity of N-[2-(Benzothiazol-2-Sulfonyl)-1-Ethoxyethoxy]- 5-(Benzothiazol-2-Ylsulfanyl)Pentanamidine." Latvian Journal of Chemistry 51, no. 1-2 (2012): 149–53. http://dx.doi.org/10.2478/v10161-012-0003-1.

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Unusual Synthesis and Cytotoxicity of N-[2-(Benzothiazol-2-Sulfonyl)-1-Ethoxyethoxy]- 5-(Benzothiazol-2-Ylsulfanyl)PentanamidineAddition of N-hydroxy-5-(benzothiazolylthio)pentanamidine toE-2-(2-chlorovinylsulfonyl)benzothiazole in the presence of NaH was studied. The main product of reaction - N-[2-(benzothiazol-2-sulfonyl)-1-ethoxyethoxy]-5-(benzothiazol-2-ylsulfanyl)pentanamidine exhibits high cytotoxicity.

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2

Arafat, Mahmoud, Ehab Abdel-Latif, Fathy M. El-Taweel, Seif-Eldin N. Ayyad, and Khaled S. Mohamed. "Synthesis and biological assessment of new benzothiazolopyridine and benzothiazolyl- triazole derivatives as antioxidant and antibacterial agents." Bulletin of the Chemical Society of Ethiopia 36, no. 2 (2022): 451–63. http://dx.doi.org/10.4314/bcse.v36i2.17.

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ABSTRACT. A novel series of benzothiazolopyridine derivatives was synthesized via interaction of -2-(benzothiazol-2-yl)-3-(4-chlorophenyl)acrylonitrile (2) with a diverse of commercially available reagents (indandione, thiobarbituric acid, and malononitrile). Moreover, a novel group of benzothiazole linked substituted 1,2,3-triazole derivatives were synthesized by exploring the chemical behavior of 5-benzothiazolyl-2-(4-chlorophenyl)-triazol-4-amine through refluxing in glacial acetic acid, condensation with phthalic anhydride, and cyanoacetylation reactions. All newly synthetized compounds ha

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3

K. Jassim, Ibtisam, Sawsan S. Harth, Rua M. Dhedan, and Ali Obais Abd. "Synthesis and study the biological activity of some six, five and fused ring heteroatome systems derived from 2-mercapto benzothiazole." Tikrit Journal of Pharmaceutical Sciences 8, no. 1 (2023): 96–105. http://dx.doi.org/10.25130/tjphs.2012.8.1.12.96.105.

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In this paper ,new series of 2-hydrazino benzothiazole [1], 2-N-benzothiazole-N`-phenyl hydrazine carboxamide [2], 2-N-[(3)-N`-phenyl-5-(p-bromophenyl)-2`-hydroxy-1,3-oxazolin-2`-yl] benzothiazol hydrazine [3] , 2-N-benzothiazole-N`-1-naphthyl hydrazine carboxamide [4], 2-N-[(3`)-N`-(1-naphthyl)-5`-(p-bromo phenyl)-2`-hydroxy-1,3-oxazolin-2`-yl)] benzothiazol hydrazine [5], of 2-thiaacetic acid benzothiazole [6] ,2-thiaacetyl chloride benzothiazole [7], 5-amino-2-mercapto-1,3,4-thiadiazole [8], of 2-mercapto-[5-acetamid thiamethyl benzothiazol]-1,3,4-thiadiazole [9], 2-phenyl-5-chloromethyl-1,

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P., ANITHA, SRIDEVI G., and KONDAL REDDY K. "Synthesis of 1-Benzothiazol-2-yl-2-arylimino-striazolo [ 5, 1-b ]benzothiazoles." Journal of Indian Chemical Society Vol. 72, Apr 1995 (1995): 257–59. https://doi.org/10.5281/zenodo.5902215.

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Department of Chemistry, Osmania University, Hyderabad-500 007 <em>Manuscript received 19 October 1993, accepted 20 December 1993</em> <em>N</em>-Aryl-<em>N',N"</em>-bis(benzothiazol-2-yl)guanidines have been obtained by the reaction of <em>N</em>-aryl-<em>N'</em>-benzothiazol-2-ylthioureas (1) with lead oxide. Oxidative cyclisation of N-aryl-<em>N'</em> ,<em>N"</em>-bis(benzothiazol-2-yl)guanidines (2) by lead tetraacetate led to the formation of 1-benzothiazol-2-yl-2-arylimino-s-triazolo[5,1-b]benzothiazoles (5).

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5

Anuba, C., and T. F. Abbs Fen Reji. "Synthesis, Characterization and Biological Activities of Substituted 1-[Benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-ones." Asian Journal of Organic & Medicinal Chemistry 4, no. 3 (2019): 144–46. http://dx.doi.org/10.14233/ajomc.2019.ajomc-p181.

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A series of ortho and para substituted 1-[benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-one derivatives were synthesized from 2-acetyl benzothiazole and ortho and para-substituted benzaldehye using ethanol as solvent. The synthesized compounds were characterized by UV-visible, FT-IR, 1H NMR and mass spectrometry. Antioxidant activities of synthesized compounds have been evaluated by DPPH free radical scavenging activity using ascorbic acid as standard. The standard solution and 1-[benzothiazol- (1H)-2-yl]-3-phenylprop-2-en-1-ones compounds were prepared with different concentrations. Anticancer

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Yavari, Issa, Kiyana Ghafouri, Maryam Naeimabadi, and Mohammad Halvagar. "A Synthesis of Functionalized 2-Indolizin-3-yl-1,3-benzothiazoles from 1-(1,3-Benzothiazol-2-ylmethyl)pyridinium Iodide and Acetylenic Esters." Synlett 29, no. 02 (2017): 243–45. http://dx.doi.org/10.1055/s-0036-1590910.

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Functionalized 2-indolizin-3-yl-1,3-benzothiazoles were obtained in moderate yields from the reaction between 1-(1,3-benzothiazol-2-ylmethyl)pyridinium iodide and acetylenic esters in acetonitrile. When isoquinoline was used under similar conditions, dialkyl 3-(1,3-benzothiazol-2-yl)pyrrolo[2,1-a]isoquinoline-1,2-dicarboxylates were obtained. The structures of these products have been confirmed by X-ray diffractometry.

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Amosova, Svetlana V., Vladimir A. Shagun, Nataliya A. Makhaeva, Irina A. Novokshonova, and Vladimir A. Potapov. "Quantum Chemical and Experimental Studies of an Unprecedented Reaction Pathway of Nucleophilic Substitution of 2-Bromomethyl-1,3-thiaselenole with 1,3-Benzothiazole-2-thiol Proceeding Stepwise at Three Different Centers of Seleniranium Intermediates." Molecules 26, no. 21 (2021): 6685. http://dx.doi.org/10.3390/molecules26216685.

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The results of quantum chemical and experimental studies of the reaction of 2-bromomethyl-1,3-thiaselenole with 1,3-benzothiazole-2-thiol made it possible to discover the unprecedented pathway of this reaction, which proceeds stepwise at three different centers of seleniranium intermediates. The first stage includes an attack of thiolate anion at the selenium atom of the seleniranium cation accompanied by ring opening with the formation of (Z)-2-[(1,3-benzothiazol-2-ylsulfanyl)selanyl]ethenyl vinyl sulfide, which is converted to six-membered heterocycle, 2-(2,3-dihydro-1,4-thiaselenin-2-ylsulf

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Lystsova, Ekaterina A., Alexander S. Novikov, Maksim V. Dmitriev, Andrey N. Maslivets, and Ekaterina E. Khramtsova. "Approach to Pyrido[2,1-b][1,3]benzothiazol-1-ones via In Situ Generation of Acyl(1,3-benzothiazol-2-yl)ketenes by Thermolysis of Pyrrolo[2,1-c][1,4]benzothiazine-1,2,4-triones." Molecules 28, no. 14 (2023): 5495. http://dx.doi.org/10.3390/molecules28145495.

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Acyl(imidoyl)ketenes are highly reactive heterocumulenes that enable diversity-oriented synthesis of various drug-like heterocycles. Such ketenes, bearing heterocyclic substituents, afford angularly fused pyridin-2(1H)-ones in their [4+2]-cyclodimerization reactions. We have utilized this property for the development of a new synthetic approach to pharmaceutically interesting pyrido[2,1-b][1,3]benzothiazol-1-ones via the [4+2]-cyclodimerization of acyl(1,3-benzothiazol-2-yl)ketenes generated in situ. The thermal behaviors of 3-aroylpyrrolo[2,1-c][1,4]benzothiazine-1,2,4-triones and 3-benzoylpy

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9

Dai, Yanling, Chen Xie, Lingmin Wu, et al. "Asymmetric synthesis of amino-benzothiazol derivatives by additions of 2-lithiated benzothiazoles to (S)-N-t-butylsulfinyl-ketimines." RSC Advances 5, no. 5 (2015): 3491–97. http://dx.doi.org/10.1039/c4ra15405c.

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We reported the asymmetric Mannich reactions between lithium-benzothiazoles and (S)-N-tert-butanesulfinylketimines, which gave unknown type of amino-benzothiazol derivatives of high pharmaceutical potential with up to 96% yields and 99 : 1 diastereoselectivities.

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Zhang, Chao, Juan Xu, Xinyu Zhao, and Congmin Kang. "Synthesis of Novel 3-(Benzothiazol-2-Ylmethylene)Indolin-2-Ones." Journal of Chemical Research 41, no. 9 (2017): 537–40. http://dx.doi.org/10.3184/174751917x15040891974776.

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A mild method for the synthesis of 3-(benzothiazol-2-ylmethylene)indolin-2-ones via the aldol condensation of substituted indolin-2-ones and benzothiazole-2-carbaldehyde is described. This new procedure has significant advantages, such as mild conditions, high yields and simple work-up.

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Dissertations / Theses on the topic "Benzothiazol"

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Fischer, Andreas [Verfasser], Manfred [Akademischer Betreuer] Braun, and Thomas J. J. [Akademischer Betreuer] Müller. "Synthese neuer Kaliumkanalöffner mit Benzothiadiazin-, Benzothiazol-, Benzodithiepin-, Thiochromanon- und Isothiochromanon-Gerüst / Andreas Fischer. Gutachter: Manfred Braun ; Thomas J. J. Müller. Betreuer: Manfred Braun." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2014. http://d-nb.info/1053467346/34.

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2

Heider, Silvio. "Synthese neuer tri- und hexadentater Stickstoffbasen für Eisen(II) Spin Crossover Komplexe." Doctoral thesis, Universitätsbibliothek Chemnitz, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-120783.

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Die vorliegende Arbeit thematisiert Eisen(II)-Komplexe mit Spinübergangseigenschaften. Dafür wurden neue hexadentate Liganden auf Basis von N,N'-Bis(2,2'-bipyridin-6-ylmethyl)-2,2'-biphenylendiamin entwickelt. Die in Kapitel 3.1 vorgestellten Systeme variieren dabei in den jeweiligen Substituenten der 6,6‘-Positionen der Biphenyleinheit. Es wird der Einfluss dieser Gruppen auf die magnetischen Eigenschaften der resultierenden Komplexe gezeigt. Im darauffolgenden Kapitel 3.2 wird ein variiertes Ligandensystem vorgestellt, in welchem anstelle einfacher Substituenten Donorfunktionen eingeführt wu

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3

Fowler, Anne Michelle. "Metabolism of benzothiazole." Thesis, University of Hertfordshire, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314573.

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4

Schmidt, Claas [Verfasser], and Horst [Akademischer Betreuer] Lemoine. "Charakterisierung neuartiger K(ATP)-Kanalöffner vom Benzothiadiazin-, Benzofuran-, Benzothiophen- und Benzothiazol-Typ an HEK 293-(SUR2B/Kir6.1)- und CHO-(SUR1/Kir6.2)-Zellen - Funktioneller Nachweis einer dritten Bindungsstelle für Benzothiadiazin-Derivate am (SUR2B/Kir6.1)-K(ATP)-Kanal / Claas Schmidt. Gutachter: Horst Lemoine." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2015. http://d-nb.info/1071947117/34.

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5

Blunt, Christoper Edward. "The synthesis of benzisothiazole and benzothiazole natural products." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/49541/.

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Chapter 1 gives an introduction to benzisothiazole and benzothiazole natural products. It explores the scope of natural products that are known within these families and discusses what they are used for, how they have been made and how they may have been biosynthesised. Chapter 1 provides a review of each family of natural products in turn. Chapter 2 describes the total synthesis of the benzisothiazole natural products aulosirazole and pronqodine A, and a series of unnatural analogues. The Chapter begins with a short discussion on the use of the Diels-Alder reaction for the formation of naphth

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Billeau, Sébastien. "Synthèse de molécules dérivées du benzothiazole et de la tétrahydroacridine." Aix-Marseille 3, 2004. http://www.theses.fr/2004AIX30033.

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Au cours de ce travail, nous avons développé la synthèse d’une nouvelle famille de composés : les thiazolo-tétrahydroacridines. Une stratégie de synthèse a été élaborée puis optimisée et nous avons ainsi obtenu huit molécules originales. De nombreux composés benzothiazoliques préparés au cours de ce travail en tant qu’intermédiaires de synthèse, présentent, eux aussi, un intérêt certain. Ceci nous a permis de valoriser ces produits. Tous les composés synthétisés sont en cours d’évaluation dans différents domaines d’activité et notamment dans le domaine thérapeutique. Certains résultats au nive

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Potter, Charles Alan Stuart. "Excited state proton transfer in 2-substituted benzothiazoles." Thesis, University of Central Lancashire, 1993. http://clok.uclan.ac.uk/19742/.

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The photophysics of 2-(2'-hydroxyphenyl)benzothiazole (HBT) and related compounds has been studied as a function of solvent, pH or H 0 and temperature. Measurements of absorption and fluorescence spectra and fluorescence decay profiles under these various conditions have been combined with theoretical calculations to arrive at an understanding of the excited state behaviour of HBT and derivatives. An investigation has been made into the protonation and deprotonation of 2-phenylbenzothiazole, 2-(2'-methoxyphenyl)benzothiazole), HBT and derivatives of HBT with bromine, chlorine, hydroxy, methoxy

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Bunescu, Andrei. "Photo-et biodégradation de dérivés du benzothiazole : étude en système combiné." Phd thesis, Université Blaise Pascal - Clermont-Ferrand II, 2006. http://tel.archives-ouvertes.fr/tel-00713567.

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La dégradation en solution aqueuse du 2-aminobenzothiazole (ABT) et du benzothiazole (BT) a été étudiée par voies photochimique, microbiologique et en combinant les deux approches. La voie photochimique impliquait des complexes aqueux de fer ou le complexe entre le fer et l'acide nitrilotriacétique (FeNTA). La voie microbiologique utilisait une souche bactérienne de Rhodococcus rhodochrous. Les schémas de dégradation ont été établis pour les différentes voies. Nous avons montré qu'il existait une grande similitude entre la dégradation photochimique et microbiologique. De plus, deux nouveaux pr

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9

Paranjpe, Shirish. "Synthesis of Novel Fluorescent Benzothiazole Cyanine Dyes as Potential Imaging Agents." Digital Archive @ GSU, 2012. http://digitalarchive.gsu.edu/chemistry_theses/55.

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Near-infrared (NIR) fluorescence imaging has emerged as an attractive non-invasive approach for direct visualization of diseases which depends on the development of stable, highly specific and sensitive optical probes. The NIR region of the electronic spectrum offers a reduction in the background autofluorescence and an increase in the tissue penetration depth. Cyanine dyes have often been considered promising contrast optic agents owing to their photophysical properties. Herein the synthesis of various penta- and heptamethine benzothiazole cyanine dyes has been described and their in vivo ima

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Willis, Kimberlee Susan. "Developing benzothiazole functionalised ruthenium(II) polypyridyl complexes as tuneable DNA binders." Thesis, Queen's University Belfast, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675442.

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The aim of this research is to develop a range of new ruthenium(II) polypyridyl complexes to be analysed spectroscopically in the presence of calf thymus-DNA to determine their relative binding affinities to the polynucleotide, thus determining the best criteria for a detection tool for DNA. Reactions of selected functional groups on one ligand of ruthenium(II) precursor complexes lead to the synthesis of six benzothiazole containing complexes; [Ru(bpY)2(B16)]2+,, [Ru(bpy)2(P5)]2+, [Ru(phen)2(B16)]2+, [Ru (phenh(P5)]2+, [Ru(Me2bpY)2(B16)]2+ and [Ru(Me2bpy)2(P5)]2+ and four "control" complexes;

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Books on the topic "Benzothiazol"

1

Heijstek, Atakan. Benzothiazole: Preparation, Structure and Uses. Nova Science Publishers, Incorporated, 2020.

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Heijstek, Atakan. Benzothiazole: Preparation, Structure and Uses. Nova Science Publishers, Incorporated, 2020.

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3

Shaikh, Faiyazalam, and Navin Patel. Benzothiazole. Biologically Useful and Important Scaffold. GRIN Verlag GmbH, 2018.

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4

Fernandez, Jose Miguel Aurrecoechea. Pyridine and benzothiazole derivatives in carbanionic reactions. 1985.

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5

Drewniak-Deyrup, Malgorzata. Some applications of benzotriazole as a synthetic auxiliary. 1988.

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Bhat, Mahesh, and S. L. Belagali, eds. In-Silico and In-Vitro Approaches to Screen the Antituberculosis Activity of Benzothiazole Analogs. BENTHAM SCIENCE PUBLISHERS, 2021. http://dx.doi.org/10.2174/97898114946351210101.

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Singh, Rajesh Kumar, ed. Key Heterocyclic Cores for Smart Anticancer Drug–Design Part I. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150400741220101.

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This book provides an update on heterocyclic compounds that serve as key components of anti-cancer agents administered in pre-clinical settings. Many of the compounds highlighted in the book are being actively investigated for the bioactive properties against a range of cancer cell lines. There is potential for heterocyclic compounds to design agents that can target specific molecules to treat different types of cancers. Chapters are contributed by experts in pharmaceutical chemistry and are written to give a general overview of the topic to readers involved in all levels of research and decis

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Kreher, Mareta. 2,3-Dihydro-pyrrolo[2,1-b]oxazole, 2,3-Dihydro-pyrrolo[2,1-b]thiazole, 2-Aryl-pyrrolo[2,1-b]benzothiazole und 2,3-Dihydro-1H-pyrrolizine: Synthese, Analytik und Testung der antiinflammatorischen Wirksamkeit sowie der modifizierte HET-CAM-Test als Modell zur Bestimmung der antiphlogistichen und antirheumatischen Wirksamkeit von Arzneistoffen. 1995.

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Book chapters on the topic "Benzothiazol"

1

Engler, Henry, William Klunk, Agneta Nordberg, et al. "First PET Study with a Benzothiazol Amyloidimaging Agent (PIB) in Alzheimer’s Disease Patients and Healthy Volunteers." In The Living Brain and Alzheimer’s Disease. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-59300-0_10.

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Wang, Yonggang, Tianhui Ren, and Jiusheng Li. "Tribological Studies on a Novel Borate Ester Containing Benzothiazol-2-yl and Disulfide Groups as EP and Multifunctional Additive." In Advanced Tribology. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03653-8_305.

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Wu, Yong-Jin. "Thiazoles and Benzothiazoles." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2012_78.

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Rauf, Abdul, and Nida Nayyar Farshori. "Benzimidazoles, Benzothiazoles and Benzoxazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_10.

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Klunk, William E., Yanming Wang, and Chester A. Mathis. "Development of Benzothiazole Amyloid-Imaging Agents." In The Living Brain and Alzheimer’s Disease. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-59300-0_9.

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Bhatia, Rohan, Preeti Ashokkumar Chaudhran, and Abha Sharma. "Benzothiazole-Based Fluorescent Probes for Various Applications." In Small Organic Molecules-Based Fluorescent Biosensors and their Applications. CRC Press, 2025. https://doi.org/10.1201/9781032706245-11.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of 1,3,2-benzothiazolyl radical." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23675-4_4709.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetracyanonotrosylchromate(I) complex with benzothiazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_461.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with benzothiazole-2-carboxyhydrazide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_272.

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Desai, Kishor R., Vedant Patel, Misha Patel, Bhavin R. Patel, and Anand J. Patel. "Synthesis and Biological Evaluation of Benzothiazepine, Benzothiazole, and Benzothiophene Derivatives." In S-Heterocycles. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-4308-7_6.

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Conference papers on the topic "Benzothiazol"

1

Lukovits, I., T. Kosztolányi, E. Kálmán, and G. Pálinkás. "Corrosion Inhibitors: Correlation between Chemical Structure and Efficiency." In CORROSION 1999. NACE International, 1999. https://doi.org/10.5006/c1999-99242.

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Abstract Corrosion inhibition efficiencies of heterocyclic, aromatic or partially saturated aromatic compounds (pyrimidines, benzothiazole derivatives, amino-acids containing an aromatic part, pyridines and quinolines) were correlated with quantum chemical indices of the respective molecules. Inhibition efficiencies measured in acidic solutions containing 0.001 and 0.01 mol/L of the inhibitor, respectively, were collected. The quantum chemical calculations were done by using the simple Hückel method. Comparison of inhibition efficiencies and the differences between energies of the highest occu

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Papavlassopoulos, H., G. Ostendorp, D. Riemer, K. Ehring, and C. Röhl. "Zum Vorkommen von Benzothiazol in der Innenraumluft öffentlicher Gebäude und dessen Abhängigkeit vom Fußbodenmaterial." In Der Öffentliche Gesundheitsdienst: Mitten in der Gesellschaft. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1679400.

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TANIMURA, M., N. WATANABE, H. K. IJUIN, and M. MATSUMOTO. "SOLVENT-PROMOTED CHEMILUMINESCENT DECOMPOSITION OF BICYCLIC DIOXETANES BEARING A 4-(BENZOTHIAZOL-2-YL)-3-HYDROXYPHENYL." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0032.

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Cabrera, José, Mateo Alajarín, and Aurelia Pastor. "Dimeric Anhydro Bases from Benzothiazole Derivatives." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01402.

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Ha, Sie-Tiong, Guan-Yeow Yeap, Teck-Leong Lee, and Teck-Ming Koh. "New Heterocyclic Liquid Crystals with Benzothiazole Core." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00373.

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Bhagdev, Khyati, and Sibaji Sarkar. "Benzothiazole Moiety and Its Derivatives as Antiviral Agents." In ECMS 2021. MDPI, 2021. http://dx.doi.org/10.3390/ecms2021-10839.

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Blaja, Svetlana, Aculina Aricu, Kaleria Kuchkova, and Alic Barba. "Synthesis of some new homodrimane derivatives of benzothiazole from norambreinolide." In New frontiers in natural product chemistry, scientific seminar with international participation. Institute of Chemistry, 2021. http://dx.doi.org/10.19261/nfnpc.2021.ab26.

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8

Uma, Pathki, Firasath Unnisa, Pallati Naresh, Sai Prakash, P. R. Sushma, and Kamatala Chinna Rajanna. "Synthesis, characterization and biological activity of benzothiazoles derivatives." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON PHYSICS OF MATERIALS AND NANOTECHNOLOGY ICPN 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0009036.

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9

Alasadi, Rahman Tama Haiwal, Noralhuda M. A. Alhussein, and Zeid Hassan Abood. "Synthesis and preliminary antibacterial activities of novel benzothiazoles." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0027666.

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10

Ha, Sie-Tiong, Hong-Cheu Lin, Guan-Yeow Yeap, Siew-Teng Ong, and Teck-Ming Koh. "Synthesis and Mesogenic Properties of New Schiff Bases Comprising Benzothiazole Moiety." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00168.

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Reports on the topic "Benzothiazol"

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Steele, W. V., R. D. Chirico, S. E. Knipmeyer, and A. Nguyen. The thermodynamic properties of benzothiazole and benzoxazole. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5364366.

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2

Tsai, Tsu-Tzu, and Fred E. Arnold. Synthesis and Properties of Rigid-Rod Benzobisazole Polymers Containing Benzothiazole Pendent Groups. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada234742.

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