Relevant bibliographies by topics / 4-dithiazole

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Academic literature on the topic '4-dithiazole'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "4-dithiazole"

1

Tsaplin, G. V., E. I. Bashkalova, A. L. Alekseenko, and S. V. Popkov. "Synthesis of azole derivatives of 1,2,3-dithiazole-5-imines and study of their fungicidal." Журнал общей химии 93, no. 12 (2023): 1846–53. http://dx.doi.org/10.31857/s0044460x23120041.

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A three-stage method was proposed for the synthesis of new 4-[4-(2-azolylethyl)piperazine-1-yl]- N -aryl-5 H 1,2,3-dithiazole-5-imines. This approach includes the reaction of Appel salt with anilines to produce 1,2,3-dithiazole-5-imines, which were converted into 4-[(4-chloroethyl)piperazine-1-yl]-5 H -1,2,3-dithiazole-5-imines, alkylating azoles at the final stage. The high fungicidal activity of target compounds and intermediate 4-chloro N -aryl-1,2,3-dithiazole-5-imines was shown in vitro tests versus six species of phytopathogenic fungi.
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Tsaplin, G. V., E. I. Bashkalova, A. L. Alekseenko, and S. V. Popkov. "Synthesis of Azole Derivatives of 1,2,3-Dithiazole-5-imines and Study of Their Fungicidal." Russian Journal of General Chemistry 93, no. 12 (2023): 3055–61. http://dx.doi.org/10.1134/s1070363223120046.

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Abstract A three-stage method was proposed for the synthesis of new 4-[4-(2-azolylethyl)piperazine-1-yl]-N-aryl-5H-1,2,3-dithiazole-5-imines. This approach includes the reaction of Appel salt with anilines to produce 1,2,3-dithiazole-5-imines, which were converted into 4-[(4-chloroethyl)piperazine-1-yl]-5H-1,2,3-dithiazole-5-imines, alkylating azoles at the final stage. The high fungicidal activity of target compounds and intermediate 4-chloro-N-aryl-1,2,3-dithiazole-5-imines was shown in vitro tests versus six species of phytopathogenic fungi.
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3

Constantinides, Christos P., Maria Koyioni, Fadwat Bazzi, Maria Manoli, Daniel B. Lawson, and Panayiotis A. Koutentis. "Crystal Structure and Solid-State Packing of 4-Chloro-5H-1,2,3-dithiazol-5-one and 4-Chloro-5H-1,2,3-dithiazole-5-thione." Molecules 26, no. 19 (2021): 5875. http://dx.doi.org/10.3390/molecules26195875.

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The crystal structure and solid-state packing of 4-chloro-5H-1,2,3-dithiazol-5-one and two polymorphs of 4-chloro-5H-1,2,3-dithiazole-5-thione were analyzed and compared to structural data of similar systems. These five-membered S,N-rich heterocycles are planar with considerable bond localization. All three structures demonstrate tight solid-state packing without voids which is attributed to a rich network of short intermolecular electrostatic contacts. These include Sδ+…Nδ−, Sδ+…Oδ−, Sδ+…Clδ− and Sδ+…Sδ− interactions that are well within the sum of their van der Waals radii (∑VDW). B3LYP, BLY
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4

Oakley, R. T., H. Koenig, and A. W. Cordes. "Structure of 1,3,2-dithiazole-4-thione." Acta Crystallographica Section C Crystal Structure Communications 43, no. 12 (1987): 2468–69. http://dx.doi.org/10.1107/s0108270187087298.

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5

D.T.Tayade*, R. D. Thombare S.A. Waghmare. "SYNTHESIS OF 3-[4-AMINO-N-SUBSTITUTED-o-ANISAMIDO- 5-YL]AMINO-5-SUBSTITUTED-1,2,4-DITHIAZOLE." Indo American Journal of Pharmaceutical Sciences 04, no. 10 (2017): 3890–94. https://doi.org/10.5281/zenodo.1035231.

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A novel series of 3-{4-Amino-N-[2-(dithethylamino)ethyl-o-anisamido-5-yl}amino-5-substitutedimino-1,2,4- dithiazole was synthesized by the oxidative cyclization of 4-amino-5-substituteddithiobiureto-N-[2- (dithethylamino)ethyl-o-anisamide in chloroform medium by making the use of liquid bromine as oxidizing agent. The products were characterized and justified on the basis of elemental analysis, chemical characteristics and spectral studies. Keywords:3-{4-Amino-N-[2-(dithethylamino)ethyl-o-anisamido-5-yl}amino-5-substituted -imino-1,2,4-dithiazole, 4- amino-5-substituteddithiobiureto-N-[2-(dith
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6

Lynch, Daniel E., and Ian McClenaghan. "6-Amino-4-iminio-4H-1,3,5-dithiazole iodide." Acta Crystallographica Section E Structure Reports Online 57, no. 1 (2000): o70—o71. http://dx.doi.org/10.1107/s160053680002047x.

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The structure of the title compound, C3H6IN3S2, comprises a puckered ring that associates to the I−anionviaN—H...I interactions. In the asymmetric unit, two I−anions reside on special positions (twofold rotation axes) equivalent to one complete anion per cation. The cationic charge is delocalized between the two amines, as suggested by the similar bond lengths, across the heterocyclic N atom, between these two groups.
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7

Cordes, A. Wallace, James R. Mingie, Richard T. Oakley, Robert W. Reed, and Hongzhou Zhang. "Quinoxaline-1,2,3-dithiazolyls — Synthesis, EPR characterization, and redox chemistry." Canadian Journal of Chemistry 79, no. 9 (2001): 1352–59. http://dx.doi.org/10.1139/v01-122.

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Oxidation of quinoxalineaminothiol with SCl2 or S2Cl2/Cl2 affords a series of compounds based on the quinoxaline-1,2,3-dithiazole framework QDTA. Under highly oxidizing conditions, the 1,2,3-dithiazolyl ring is opened to afford the acyclic dichlorosulfimino-sulfenyl chlorides Clx-QDTA-Cl3 (x = 0, 1, 2). Reduction of these "trichloro" compounds leads to ring closure. For x = 2, reduction using S2Cl2 affords the dithiazolylium chloride [Cl2-QDTA][Cl]. For all values of x, reduction with iodide ion (3 mol equiv) affords the corresponding dithiazolyl radical [Clx-QDTA]. The radicals can be isolate
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8

Yarovenko, Vladimir N., Andrey A. Es'kov, George V. Zatonsky, et al. "Synthesis of azomethylene derivatives of 4-chloro-5H-1,2,3-dithiazole." Journal of Heterocyclic Chemistry 41, no. 1 (2004): 37–43. http://dx.doi.org/10.1002/jhet.5570410106.

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9

Yokoyama, Masataka, Tadashi Shiraishi, Hidekatsu Hatanaka, and Koreharu Ogata. "Synthesis and structure determination of [1,2]dithiolo[1,5-b][1,2,4]dithiazole-4-S IV derivatives." Journal of the Chemical Society, Chemical Communications, no. 23 (1985): 1704. http://dx.doi.org/10.1039/c39850001704.

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10

Gdaniec, Maria, Krzysztof Osmialowski, and Franciszek Saczewski. "Crystal and molecular structure of 3-(4-chlorobenzoylimino)-5,6-dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole." Journal of Crystallographic and Spectroscopic Research 19, no. 3 (1989): 507–12. http://dx.doi.org/10.1007/bf01185387.

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Book chapters on the topic "4-dithiazole"

1

Argyropoulos, N. G. "Mesoionic 1,3,2-Dithiazol-4-ones by Oxidation of 1,3,2-Dithiazole-4-thiones." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00111.

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Yarovenko, V. N., A. A. Eskov, I. V. Zavarzin, and M. M. Krayushkin. "Synthesis of 4-Chloro-5H-l,2,3-Dithiazole Azomethylene Derivatives." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50363-4.

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Argyropoulos, N. G. "5-Amino-1,3,2-dithiazole-4-thiones from 1,3,2-Dithiazolium Salts." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00110.

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Argyropoulos, N. G. "Mesoionic 1,3,2-Dithiazole-4-thiones from 1,3,2-Dithiazolium Salts and Vice Versa." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00109.

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Argyropoulos, N. G. "Mesoionic 1,3,2-Dithiazole-4-thiones from Alkynes and 1,2,4,6-Tetrathia-3,5,7-triazepinium Chloride." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00105.

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Argyropoulos, N. G. "Mesoionic 1,3,2-Dithiazol-4-imines from Phenylacetylene and Tetrasulfur Tetranitride." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00104.

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7

Kikelj, D. "From 2-[(4-Chloro-5-1,2,3-dithiazol-5-ylidene)amino]benzonitrile." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00837.

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8

Kantlehner, W. "Synthesis from 5-(4-Chloro-5-1,2,3-dithiazol-5-ylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00413.

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Journal articles
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