Relevant bibliographies by topics / Benzisothiazol

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Benzisothiazol'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Benzisothiazol"

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McKinnon, David M., and Kingsley R. Lee. "Fused heterocycles from o-acylbenzenethiol derivatives." Canadian Journal of Chemistry 66, no. 6 (1988): 1405–9. http://dx.doi.org/10.1139/v88-227.

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The oximes of 2-acylthioanisole derivatives may be conveniently converted into 1,2-benzisothiazoles by acetic anhydride in pyridine. 3-(2-Methylthiophenyl)-1,2-benzisothiazole, prepared by this method, has been further converted into the 1,2-benzisothiazolo[2,3-b]-1,2-benzisothiazolium system. The phenylhydrazones of certain 2-acylthioanisoles are also cyclized by polyphosphoric acid to 2-(2-methylthio)phenylindoles, which are further converted into benzo[b]thieno[3,2-b]indoles by demethylation and oxidation.
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McKinnon, David M., K. Ann Duncan, Aileen M. McKinnon, and Perry A. Spevack. "The preparation of some fused isothiazole derivatives." Canadian Journal of Chemistry 63, no. 4 (1985): 882–86. http://dx.doi.org/10.1139/v85-146.

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The treatment of di(2-amino-5-methylphenyl)methane with N-sulfinylmethanesulfonamide gives two materials, 3-(2-amino-5-methylphenyl)-5-methyl-2,1-benzisothiazole and what appears to be its tautomer, a 2,1-benzisothiazolo[2,3-b]-2,1-benzisothiazole derivative. Reaction of the former with methyl iodide gives mono-, di-, and trimethyl derivatives. The second of these also possesses the symmetrical 2,1-benzisothiazolo[2,3-b]-2,1-benztsothiazole structure. The structure of the other methylation product and of the acetylation products are discussed. Some 1,2-dithiol-3-ylidene-2-pyridylmethanes were
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Ramezanpour, Sorour, Zahra Bigdeli, Nahid Alavijeh, and Frank Rominger. "Application of Saccharin as an Acidic Partner in the Ugi Reaction for the One-Pot Synthesis of 3-Iminosaccharins." Synlett 28, no. 10 (2017): 1214–18. http://dx.doi.org/10.1055/s-0036-1558962.

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The use of saccharin as a replacement for the carboxylic acid component in an Ugi multicomponent condensation leading to [(1,1-dioxido-1,2-benzisothiazol-3-yl)amino]acetamide (3-iminosaccharin) derivatives is described for the first time.
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Li, Ting, Lei Yang, Kaidong Ni, Zhenyu Shi, Fei Li, and Dongyin Chen. "An efficient approach to construct benzisothiazol-3(2H)-ones via copper-catalyzed consecutive reaction of 2-halobenzamides and carbon disulfide." Organic & Biomolecular Chemistry 14, no. 26 (2016): 6297–303. http://dx.doi.org/10.1039/c6ob00819d.

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An efficient copper-catalyzed reaction for the synthesis of benzisothiazol-3(2H)-ones has been developed, starting from easily available 2-halobenzamides and carbon disulfide. The reaction proceeds via a consecutive process with S–C bond and S–N bond formation.
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G., S. SADANA, S. PRADHAN NITIN, and D. DEODHAR K. "Synthesis and Antibacterial Activity of 5-Arylidene-1 ,2,4-triazino [4, 3-b]-1,2-benzisothiazol- 3-one-6,6-dioxides." Journal of Indian Chemical Society Vol. 67, Oct. 1990 (1990): 861–62. https://doi.org/10.5281/zenodo.6279048.

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Department of Chemistry, G. N. Khalsa College, Bombay-400 019 Department of &nbsp;Chemistry, Indian Institute of &nbsp;Technology, Bombay-400 076 <em>Manuscript received </em>26 <em>September 1989, revised 16 July 1990, accepted 1 August 1990</em> Synthesis and Antibacterial Activity of&nbsp; 5-Arylidene-1,2,4-triazino[4,3-<em>b</em>]-1,2-benzisothiazol- 3-one-6,6-dioxides
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Banerjee, Bubun, Vaishali Bhardwaj, Amninder Kaur, Gurpreet Kaur, and Arvind Singh. "Catalytic Applications of Saccharin and its Derivatives in Organic Synthesis." Current Organic Chemistry 23, no. 28 (2020): 3191–205. http://dx.doi.org/10.2174/1385272823666191121144758.

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: Saccharin (1,2-benzisothiazol-3(2H)-one-1,1-dioxide) is a very mild, cheap, commercially available, water soluble, environmentally benign and edible Brønsted acidic substance. Recently, with other utilities, saccharin and its derivatives were employed as catalysts for various organic transformations. In this review, catalytic applicability of saccharin and its derivatives under various reaction conditions is summarized.
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Han, Hye-Jin, EunJu Kim, SunKyoung Yoo, et al. "Initial Ecological Risk Assessment of 1,2-Benzisothiazol-3-one in Environment." Journal of Korean Society of Environmental Engineers 35, no. 3 (2013): 165–70. http://dx.doi.org/10.4491/ksee.2013.35.3.165.

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Arshad, Muhammad Nadeem, Hafiz Mubashar-ur-Rehman, Muhammad Zia-ur-Rehman, Islam Ullah Khan, and Muhammad Shafiq. "2-(Prop-2-enyl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 65, no. 6 (2009): o1236. http://dx.doi.org/10.1107/s1600536809016328.

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In the title compound, C10H9NO3S, the benzisothiazole group is almost planar (with a maximum deviation of 1.61 Å). The crystal structure is stabilized by weak intermolecular C—H...O hydrogen bonds, forming a chain of molecules alongb.
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Kersting, Berthold. "Self-Assembly of Organo-Sulfur, Selenium and Tellurium Compounds via π-π-Stacking and Hydrogen Bonding Interactions". Zeitschrift für Naturforschung B 57, № 10 (2002): 1115–19. http://dx.doi.org/10.1515/znb-2002-1006.

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AbstractThe crystal structures of 2-isopropyl-benzisothiazol-3-one-7-carboxylicacid isopropyl amide and of the corresponding selenium and tellurium derivatives have been determined. In contrast to the sulfur and selenium compounds, the tellurium derivative has an unprecedented three-dimensional network structure held together via π-π stacking and hydrogen bonding interactions. The cavities in the 3D molecular network are filled with guestwater molecules that are hydrogen bonded to carbonyl oxygen atoms.
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Akpata, Ebere Immaculata, Onuabuchi Nnenna Ani, and Okwesili Fred C. Nwodo. "Phytonutrients and Anti-Nutrient Composition of Aqueous Extract of Fermented Seeds of Prosopis africana." Asian Journal of Research in Biochemistry 13, no. 3 (2023): 12–27. http://dx.doi.org/10.9734/ajrb/2023/v13i3256.

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Prosopis africana is a perennial leguminous plant in the genus Prosopis. The seeds are used as food condiment. This study was aimed at evaluating the phytochemical, proximate, vitamin and anti-nutrient compositions of aqueous extract of fermented seeds of Prosopis africana. The analyses were done using standard biochemical methods. Assessment of the bioactive constituents was carried out using gas chromatography-mass spectrometry. The result of the phytochemical analysis revealed quantifiable levels of Steroid, phenols, triterpenes, alkaloids, flavonoids, glycosides, terpenoids and saponin. Th
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Dissertations / Theses on the topic "Benzisothiazol"

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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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Vahedi, Hooshang. "Catalytic symmetric oxidation of sulfides to sulfoxides mediated by 3-substituted-1,2-benzisothiazole 1,1-dioxides." Thesis, University of Liverpool, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367257.

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Estienne, Jacques. "Des halogènes dans les édifices moléculaires étioniques : études cristallographiques, corrélations structure-réactivité, structure-conductivité, modèles structuraux." Aix-Marseille 1, 1986. http://www.theses.fr/1986AIX11001.

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Etude structurale de substances pouvant intervenir en tant que catalyseurs ou conducteurs electriques dans le monde industriel, dans le cadre de trois modeles : modele de l'atome cl mu -ponsteur co::(3) cl(c::(2)f::(3)o::(2))::(3)(so::(4))(c::(4)h::(10)o::(2))::(3) et mn::(4)cl::(4)(c::(2)f::(3)o::(2))::(4)(c::(4)h::(10)o)::(6), modele de l'ion tribromure dans des composes organiques et modele de l'iodure simple (iodures organiques comportant des dications diazoniatricycliques c::(14)h::(28)n::(2)**(2+). 2i**(-) et c::(15)h::(30)n::(2)**(2+). 2i**(-) et de l'ion iodoargentate (ag::(4) i::(8)**
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Huang, Hsin-Yu, and 黃信裕. "Facile Synthesis of Dienenitriles and 2-Aryl-1,2-benzisothiazol-3(2H)-ones Using A Hypervalent Iodine(III) Reagent." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/20370159535889908207.

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碩士<br>高雄醫學大學<br>藥學研究所<br>89<br>The Pummerer reaction of sulfoxides normally proceeds via an activa- ted sulfoxide and then a thionium ion which reacts with a nucleophile at ca- rbon to afford an -substituted sulfide. In an interrupted Pummerer reaction , the tricoordinate sulfur intermediate undergoes reaction with a nucleophile at sulfur leading to unexpected product . Recently, hypervalent iodine reagents have been used extensively in organic synthesis due to their low toxicity, ready availability and easy hand-
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Abouzeid, Azza A. "Studies on some benzisothiazole derivatives." 1990. http://hdl.handle.net/1993/17207.

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Book chapters on the topic "Benzisothiazol"

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Nutaitis, Charles F. "Isothiazoles and Benzisothiazoles." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2012_77.

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Kollenz, G. "Of 2,1-Benzisothiazol-3(1)-ones." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00385.

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Sainsbury, M. "Alkylation of 4,6-Dinitro-1,2-benzisothiazole or 4,6-Dinitro-1,2-benzisothiazol-3(2)-one." In Science of Synthesis Knowledge Updates KU 2010/4. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-111-00017.

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Brown, D. W., and M. Sainsbury. "1,2-Benzisothiazoles." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00743.

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Brown, D. W., and M. Sainsbury. "2,1-Benzisothiazoles." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00763.

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Sainsbury, M. "1,2-Benzisothiazoles." In Science of Synthesis Knowledge Updates KU 2010/4. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-111-00002.

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Sainsbury, M. "2,1-Benzisothiazoles." In Science of Synthesis Knowledge Updates KU 2010/4. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-111-00018.

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Kikelj, D. "From Benzisothiazole Derivatives." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00859.

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"The 2,1-Benzisothiazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186534.ch6.

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Unger, Thomas A. "Benzothiazoles benzothiazolines benzisothiazoles." In Pesticide Synthesis Handbook. Elsevier, 1996. http://dx.doi.org/10.1016/b978-081551401-5.50331-2.

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Conference papers on the topic "Benzisothiazol"

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Ortega, M. P., C. Sunkel, and J. G. Priego. "INHIBITION OF HUMAN PLATELET FUNCTION BY PCA-4230." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643431.

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PCA-4230 (3-{2-(N-l,2-benzisothiazolyl-3(2H)one-1,1-dioxide) ethoxycarbonyl}-2,6-dimethyl-5-ethoxycarbonyl-4-methyl-l,4-dihy-dropyridine) is a new synthetic compound which has been selected after evaluation of .several series of molecules included in an ex tensive program of synthesis and biological screening.The purpose of this study was to investigate the In vUjiO effects of PCA-4230 on human platelet function.Platelet aggregation (PA) was measured, in platelet rich plasma (PRP) or washed platelets, according to Born’s technique. Release reaction (RR) was measured by the luminiscence method
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