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Journal articles on the topic 'Dithiadiazine'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Cablewski, Teresa, Craig L. Francis, and Andris J. Liepa. "N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. VI. The Preparation of Some Fused [1,4,2,6]Dithiadiazine Dioxides." Australian Journal of Chemistry 61, no. 5 (2008): 332. http://dx.doi.org/10.1071/ch08059.

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N,N-Dialkyl-N′-chlorosulfonylchloroformamidines 1 were treated with 2-mercaptobenzimidazoles 2 to give [1,4,2,6]dithiadiazino[2,3-a]benzimidazole 1,1-dioxides 3. 3-Mercapto[1,2,4]triazoles 5 afforded [1,2,4]triazolo[2,3-b][1,4,2,6]dithiadiazine 1,1-dioxides 6 and [1,2,4]triazolo[4,3-b][1,4,2,6]dithiadiazine 1,1-dioxides 7. These products are derivatives of new or very rare heterocycles.

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2

Smits, J. M. M., P. T. Beurskens, B. G. Lenz, and B. Zwanenburg. "Structure of 3,6-bis(4-methoxyphenyl)-1,4,2,5-dithiadiazine, C16H14N2O2S2." Acta Crystallographica Section C Crystal Structure Communications 41, no. 7 (1985): 1086–87. http://dx.doi.org/10.1107/s0108270185006680.

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3

Chavan, Snehal, Baliram Berad, Avinash Ulhe, and Prajakta Waghe. "Synthesis of Bis-(N-glucosylated triazolodithiadiazinyl) alkanes using N-Glucosylated Sulfenyl Chloride Reagent." Current Chemistry Letters 14, no. 2 (2025): 373–80. https://doi.org/10.5267/j.ccl.2024.10.009.

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Methodology is reported for the synthesis of a six-membered heterocyclic ring involving cyclocondensation reaction through sulfur-sulfur bond formation. This method of synthesis allows for developing a new class of dithiadiazines. A series of bis-[6-tetra-O-acetyl-β-D-glucopyranosylimino-1,2,4-triazolo[3,4-b]-1,2,4,5-dithiadiazin-4-yl] alkanes have been synthesized by using a reagent, tetra-O-acetyl-β-D-glucopyranosylimino chloromethane sulfenyl chloride and bis-(4-amino-5-mercapto-1,2,4-triazol-3-yl) alkanes. These newly formulated N-glycosylated molecules could serve as a potential biologica

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4

Pradip, P. Deohate, and N. Berad B. "Synthesis, characterization and antimicrobial study of substituted bis-[1,2,4,5]-dithiadiazine and bis-[1,3,4]-thiadiazolidine derivatives." Journal of Indian Chemical Society Vol. 85, Oct 2008 (2008): 1050–54. https://doi.org/10.5281/zenodo.5820720.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : pradip222091@yahoo.co.in Postgraduate Department of Chemistry, Shri Shivaji Science College, Amravati-444 603, Maharashtra, India <em>Manuscript received 24 April 2008, accepted 16 July 2008</em> Series of compounds [4-(3-phenylimino-6-aryl/alkylimino-[1,2,4,5]-dithiadiazinane-4-carbonyl)-phenyl]-(3- phenylimino-6-aryl/ alkylimino-[1, 2,4, 5]-thiadiazinan-4-yI). methanones and [ 4·(2-phenylimino-5-aryl/ alkylimino· [1, 3, 4]- thiadiazolidine-3-ca

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5

Pradip, P. Deohate. "Substituted [1,2,4,5]-dithiadiazines and [1,3,4]-thiadiazolidines; synthesis, characterization and antimicrobial study." Journal of Indian Chemical Society Vol. 89, Dec 2012 (2012): 1705–10. https://doi.org/10.5281/zenodo.5772233.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 00I, Maharashtra, India <em>E-mail</em> : pradip22209l@yahoo.co.in <em>Manuscript received 12 August 2009, revised 29 February 2012, accepted 14 March 2012</em> Series of compounds 2-benzotriazol-1-yl-1-(3-phenylimino-6-aryl/alkylimino-[1,2,4,5]-dithiadiazinan-4-yl)-ethanones and 2-benzotriazol-1-yl-l-(2-phenylimino-5-aryl/alkylimino-[1,3,4]·thiadiazolidin-3-yl)-ethanones have been synthesited by the interaction of 2-benzotriazol-1-yi-<em>N</em>-aryl/alkyl thiocarbamido-acetamides with <em>N</e

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6

Pradip, P. Deohate, and R. Kawle Pravin. "Synthesis and antimicrobial screening of novel bis-triazolo-dithiadiazines containing bridgehead nitrogen." Journal of Indian Chemical Society Vol. 92, Jun 2015 (2015): 911–14. https://doi.org/10.5281/zenodo.5636751.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : pradip222091@yahoo.co.in 1,4-Bis-(3-arylimino-[1,2,4]-triazolo-[3,4-c]-[1,2,4,5]-dithiadiazin-6-yl)-benzenes have been synthesized by treating 1,4-bis-(4-amino-3-mercapto-<em>4H</em>-[1,2,4]-triazol-5-yl-benzene with <em>N-aryl</em>-S-chloro isothiocarbamoyl chlorides and then basification with dilute ammonia solution. Synthesis of 1,4-bis-(4-amino-3-mercapto-<em>4H</em>-[1,2,4]-triazol-5-yl-benzene was carried out by interacting the terephthalic acid dihydraz

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7

POTTS, K. T., and J. S. BAUM. "ChemInform Abstract: Formation of a 1,4,2,3-Dithiadiazine via Dimerization of a Transient Thione-S-imide (Thiocarbonyl Imine Dipole)." ChemInform 23, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199214239.

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8

Bryce, Martin R., Shimon Yoshida, Andrei S. Batsanov, and Judith A. K. Howard. "Thermal fragmentation reactions of 1,4,2-dithiazines and 1,4,2,5-dithiadiazines in the presence of dienophiles: synthesis of 1,4-dithiine derivatives. X-Ray crystal structures of a 1,4,2-dithiazine 1,1-dioxide and a 1,4,2,5-dithiadiazine derivative." Journal of the Chemical Society, Perkin Transactions 1, no. 8 (1997): 1157–62. http://dx.doi.org/10.1039/a606970c.

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9

Boeré, René T., Klaus H. Moock, Vicki Klassen, Joel Weaver, Dieter Lentz, and Heike Michael-Schulz. "Electrochemistry of methylidyne and 1,2,3,5-dithiadiazole complexes of iron and nickel and a reinterpretation of the composition of "PhCN2S2Fe2(CO)6"." Canadian Journal of Chemistry 73, no. 9 (1995): 1444–53. http://dx.doi.org/10.1139/v95-179.

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The title compounds have been studied in CH2Cl2 by cyclic voltammetry. Nonacarbonyldi(μ3-methylidyne)triiron, [Fe3(CO)9(μ3-CX)2] (X = F, Cl, Br, H), undergo chemically reversible 1e− reduction (−0.72 to −0.88 V vs. SCE) and irreversible oxidation (+1.59 to +1.72 V); the compound for which X = F displays a second, irreversible reduction (−1.96 V). Using reduction potentials of comparable μ3-E (E = S, Se, NPh, PPh) clusters, μ3-methylidyne ligands are shown to be strongly basic, comparable to PPh and NPh and more basic than S or Se. The methylidyne clusters are both more difficult to oxidize and

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10

Kumar Verma, Vinay, Anirudh P. Singh, and Rajendra Singh. "Synthesis of Some 6-Arylamino-3-amino-1,2,4,5-dithiadiazines." HETEROCYCLES 27, no. 10 (1988): 2373. http://dx.doi.org/10.3987/com-88-4617.

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11

Höfs, Hans-Ulrich, Jan W. Bats, Rolf Gleiter, et al. "Perhalogenierte 1,2,3,5-Dithiadiazolium-Salze und 1,2,3,5-Dithiadiazole." Chemische Berichte 118, no. 9 (1985): 3781–804. http://dx.doi.org/10.1002/cber.19851180930.

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12

Peseke, Klaus. "Synthesen mit 1,3-Dithietanen Darstellung von Perhydro-1,4,2,5-dithiadiazin-Derivaten." Zeitschrift für Chemie 21, no. 3 (2010): 102. http://dx.doi.org/10.1002/zfch.19810210305.

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13

Griffiths, Joanna, and Jeremy M. Rawson. "SYNTHESIS AND X-RAY CRYSTAL STRUCTURE OF THE ASYMMETRIC DITHIADIAZENE BrC6F4NSNSC6H4NO2." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 4-5 (2004): 883–86. http://dx.doi.org/10.1080/10426500490427754.

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14

Grekhnev, D. A., Iu V. Novikova, V. N. Yuskovets, et al. "1,2,3,4- dithiadiazole derivative 3-(4-nitrophenyl)-5-phenyl-3H-1,2,3,4-dithiadiazole-2-oxide affects both STIM1- and STIM2-dependent store-operated calcium channels." Bulletin of Experimental Biology and Medicine 179, no. 3 (2025): 268–73. https://doi.org/10.47056/0365-9615-2025-179-3-268-273.

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15

Beekman, Richard A., René T. Boeré, Klaus H. Moock, and Masood Parvez. "Synthesis, electrochemistry, structure, and magnetic susceptibility of 5-tert-butyl-1,3-bis- (1,2,3,5-dithiadiazolyl)benzene. Structural effect of the bulky substituent." Canadian Journal of Chemistry 76, no. 1 (1998): 85–93. http://dx.doi.org/10.1139/v97-213.

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The crystal structure of the title compound was determined at 250 K in space group I 4 bar 2m, a = 20.661(5) Å , c = 6.764(7) Å , Z = 8. The individual dithiadiazole rings form two sets of contrarotatory 4-member pinwheels clustered around a 4-fold rotation-inversion axis located halfway along the unit cell edges, describing an infinite channel lined with sulfur atoms but in which there are short intra-stack contacts through only one S atom of each CN2S2 group. The double-layer stacking occurs in order to accommodate the bulk of the tBu group, and the spacing between layers is very regular, wi

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16

Yamaguchi, K., T. Itoh, K. Nagata, M. Okada, and A. Ohsawa. "Two novel ten-membered ring compounds: 1,2,5,8-dithiadiazecine-6,7-diones." Acta Crystallographica Section C Crystal Structure Communications 49, no. 8 (1993): 1514–17. http://dx.doi.org/10.1107/s010827019300099x.

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17

Deohate, Pradip P. "ChemInform Abstract: Substituted [1,2,4,5]-Dithiadiazines and [1,3,4]-Thiadiazolidines; Synthesis, Characterization and Antimicrobial Study." ChemInform 44, no. 51 (2013): no. http://dx.doi.org/10.1002/chin.201351205.

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18

Van Droogenbroeck, Joris, Christian Van Alsenoy, Stephen M. Aucott, J. Derek Woollins, Allen D. Hunter, and Frank Blockhuys. "Structure, Bonding, and Reactivity of the Organometallic 1,3,2,4-Dithiadiazole Complex CpCoS2N2." Organometallics 24, no. 5 (2005): 1004–11. http://dx.doi.org/10.1021/om0494059.

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19

Pradip, P. Deohate. "Conventional and MW induced synthesis of some bridgehead nitrogen containing triazolo-dithiadiazines by sulphur-sulphur bond formation through cyclocondensation and antimicrobial study." Journal of Indian Chemical Society Vol. 94, Nov 2017 (2017): 1221–25. https://doi.org/10.5281/zenodo.5636011.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : pradip222091@yahoo.co.in <em>Manuscript received 19 July 2017, revised 11 November 2017, accepted 14 November 2017</em> Conventional and MW induced synthesis of 3-aryl/alkylimino-6-pyridin-4-yl-[1,2,4]-triazolo-(3,4-c)- [1,2,4,5]-dithiadiazines have been carried out by reacting 4-amino-3-mercapto-5-pyridin-4-yl-4<em>H-</em>[1,2,4]-triazole with N-aryl/alkyl-S-chloro isothiocarbamoyl chlorides followed by the basification with dilute ammonium hydroxide solution

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20

Yonemoto, Katsumi, and Isao Shibuya. "Decomposition Reaction of 3-Aryl-6-disubstituted Amino-1,4,2,5-dithiadiazines in the Solid State." Bulletin of the Chemical Society of Japan 62, no. 7 (1989): 2407–9. http://dx.doi.org/10.1246/bcsj.62.2407.

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21

Khairullina, Regina R., Lilya U. Dzhemileva, Vladimir A. D'yakonov, Askhat G. Ibragimov, and Usein M. Dzhemilev. "Synthesis of 1,4,2,6-dithiadiazinane 1,1-dioxide and study of its cytotoxic activity." Mendeleev Communications 32, no. 2 (2022): 178–79. http://dx.doi.org/10.1016/j.mencom.2022.03.008.

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22

YAMAGUCHI, K., T. ITOH, K. NAGATA, M. OKADA, and A. OHSAWA. "ChemInform Abstract: Two Novel Ten-Membered Ring Compounds: 1,2,5,8-Dithiadiazecine-6,7- diones." ChemInform 24, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199351043.

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23

Ulhe, A. G., S. A. Chavan, and B. N. Berad. "ChemInform Abstract: Sulfur-Sulfur Bond Formation Through Cyclo Condensation: Synthesis of Some N-Glucosylated Dithiadiazines." ChemInform 46, no. 44 (2015): no. http://dx.doi.org/10.1002/chin.201544198.

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24

Chavan, Snehal A., Avinash G. Ulhe, and Baliram N. Berad. "Synthesis and characterization of N-glucosylated dithiadiazepine derivatives through carbon-sulfur bond formation." Heterocyclic Communications 21, no. 5 (2015): 269–72. http://dx.doi.org/10.1515/hc-2015-0093.

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AbstractNew 4,7-bis(arylamino)-2-tetra-O-acetyl-β-d-glucopyranosylimino-1,3,5,6-dithiadiazepines were synthesized via reaction of N-tetra-O-acetyl-β-d-glucopyranosyl isocyanodichloride with 1,6-diaryl-2,5-dithio-bis-ureas without using any catalyst. Thus, the synthesis of 7-membered heterocycles containing two sulfur and two nitrogen atoms through carbon-sulfur bond formation was explored. The chemical structures of these new compounds were elucidated by IR, 1H NMR, 13C NMR, mass spectral, and elemental analyses.

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25

Yonemoto, Katsumi, Isao Shibuya, and Kazumasa Honda. "Formation of 1,4,2,5-Dithiadiazines as a Heterocyclic System by Reaction of 1,4,2-Dithiazolium Salts with Sulfenamides." Bulletin of the Chemical Society of Japan 61, no. 6 (1988): 2232–34. http://dx.doi.org/10.1246/bcsj.61.2232.

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26

Banister, Arthur J., Michael I. Hansford, Zdenek V. Hauptman, Simon T. Wait, and William Clegg. "Direct insertion of a nitrogen atom into the S–S bond of a 1,2,3,5- dithiadiazole ring in a direct current nitrogen glow discharge, and X-ray crystal structure of 4-methyl-1,2,3,5-dithiadiazole." J. Chem. Soc., Dalton Trans., no. 9 (1989): 1705–13. http://dx.doi.org/10.1039/dt9890001705.

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27

Nakayama, Juzo, Shuhei Iida, Yoshiaki Sugihara, and Akihiko Ishii. "Pummerer reaction of 4,7-di-tert-butyl-3h,8h-1,2,5,6-dithiadiazocine 1-oxide; formation of 1,4-dithiins." Journal of Sulfur Chemistry 25, no. 1 (2004): 13–19. http://dx.doi.org/10.1080/17415990410001658946.

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28

Rymarczyk, B. M., H. Preut, and R. P. Kreher. "An Eight-Membered N,N,S,S-Heterocyclic Compound: 4,7-Bis(4-chlorophenyl)-3,8-dihydro-1,2,5,6-dithiadiazocine." Acta Crystallographica Section C Crystal Structure Communications 53, no. 7 (1997): 931–33. http://dx.doi.org/10.1107/s0108270197002588.

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29

Lazrak, F., E. M. Essassi, Y. Kandri Rodi, K. Misbahi, and M. Pierrot. "SYNTHESE DE NOUVEAUX SYSTEMES CONDENSES RENFERMANT LE 1,2,4-TRIAZOLE, LA 1,3-THIAZINE, LA 1,3-THIAZEPINE ET LA 1,3,5,7-DITHIADIAZOCINE." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 9 (2004): 1799–808. http://dx.doi.org/10.1080/10426500490466526.

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30

Chandrasekhar, Vadapalli, Tristram Chivers, Masood Parvez, Ignacio Vargas-Baca, and Tom Ziegler. "Experimental and Theoretical Studies on 1,4,5,7-Dithiadiazepinyl Radicals: Preparation and X-ray Structure of 5-(Trimethylsilyl)tetrachlorobenzo-1,4,5,7-dithiadiazepine." Inorganic Chemistry 36, no. 21 (1997): 4772–77. http://dx.doi.org/10.1021/ic970230n.

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31

Longridge, John J., and Jeremy M. Rawson. "The syntheses and characterisation of some novel difunctional sulfur-nitrogen chains: new dithiadiazenes and trithiadiazenes derived from meta-dimercaptobenzene." Polyhedron 17, no. 11-12 (1998): 1871–75. http://dx.doi.org/10.1016/s0277-5387(97)00522-6.

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32

Risso, Vesna, Daniel Farran, Guilhem Javierre, et al. "Atropisomerism in a 10-Membered Ring with Multiple Chirality Axes: (3Z,9Z)-1,2,5,8-Dithiadiazecine-6,7(5H,8H)-dione Series." Journal of Organic Chemistry 83, no. 15 (2018): 7566–73. http://dx.doi.org/10.1021/acs.joc.8b01009.

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33

RYMARCZYK, B. M., H. PREUT, and R. P. KREHER. "ChemInform Abstract: An Eight-Membered N,N,S,S-Heterocyclic Compound: 4,7-Bis(4- chlorophenyl)-3,8-dihydro-1,2,5,6-dithiadiazocine." ChemInform 28, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199746033.

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34

Passmore, Jack, Xiaoping Sun, and Simon Parsons. "Cycloaddition reactions of SNSAsF6 with aryl nitriles and diphenylacetylene; the preparation and characterization of aryl 1,3,2,4- and 1,2,3,5-dithiadiazole radicals." Canadian Journal of Chemistry 70, no. 12 (1992): 2972–79. http://dx.doi.org/10.1139/v92-379.

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The SNS+ cation (in SNSAsF6) underwent symmetry-allowed concerted cycloadditions with the aryl nitriles RCN (R = 2,5-Me2C6H3, Ph, p-O2NC6H4, and 3,5-(O2N)2C6H3) and diphenylacetylene. The cycloadducts [Formula: see text] (R = 2,5-Me2C6H3, Ph, p-O2NC6H4, and 3,5-(O2N)2C6H3) and Ph [Formula: see text] were characterized by elemental analyses and IR and NMR (1H, 13C, 14N) spectroscopies. The reduction of [Formula: see text] gave the corresponding 1,3,2,4-dithiadiazoles [Formula: see text], which in turn rearranged to the corresponding 1,2,3,5-dithiadiazoles [Formula: see text]. The rate of this r

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35

Banister, Arthur J., Michael I. Hansford, and Zdenek V. Hauptman. "Direct insertion of a nitrogen atom into the S–S link of a 1,2,3,5-dithiadiazole ring in a D.C. nitrogen glow discharge." J. Chem. Soc., Chem. Commun., no. 2 (1987): 63–64. http://dx.doi.org/10.1039/c39870000063.

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36

PASSMORE, J., X. SUN, and S. PARSONS. "ChemInform Abstract: Cycloaddition Reactions of SNSAsF6 with Aryl Nitriles and Diphenylacetylene; the Preparation and Characterization of Aryl 1,3,2, 4- and 1,2,3,5-Dithiadiazole Radicals." ChemInform 24, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199326136.

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37

Banister, Arthur J., Ian B. Gorrell, William Clegg, and Karl Anker Jørgensen. "The 4-phenyl-1,2,3,5-dithiadiazole complex [Fe2(CO)6(PhCN2S2)]: its preparation, crystal structure, and an extended-Hückel molecular-orbital study of the bonding." J. Chem. Soc., Dalton Trans., no. 11 (1989): 2229–33. http://dx.doi.org/10.1039/dt9890002229.

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38

BRYCE, M. R., S. YOSHIDA, A. S. BATSANOV, and J. A. K. HOWARD. "ChemInform Abstract: Thermal Fragmentation Reactions of 1,4,2-Dithiazines and 1,4,2,5- Dithiadiazines in the Presence of Dienophiles: Synthesis of 1,4- Dithiine Derivatives. X-Ray Crystal Structures of a 1,4,2-Dithiazine 1, 1-Dioxide and a 1,4,2,5-Dithiad." ChemInform 28, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199736170.

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39

Banister, Arthur J., Jeremy M. Rawson, William Clegg, and Sara L. Birkby. "Preparation of salts of the 5,5′-(1,4-phenylene)bis(1,3,2,4-dithiadiazolylium) dication and of its 1,2- and 1,3-phenylene analogues. Preparation and crystal structure of the stacked, neutral 5,5′-(1,4-phenylene)bis(1,3,2,4-dithiadiazole)." J. Chem. Soc., Dalton Trans., no. 4 (1991): 1099–104. http://dx.doi.org/10.1039/dt9910001099.

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40

Wong, Wai-Kwok, Chaode Sun, Wai-Yeung Wong, Daniel W. J. Kwong та Wing-Tak Wong. "Synthesis and Chemistry of Dithiadiazole Free Radicals [4-(4′-C5H4N)CN2S2] and [4-(3′-C5H4N)CN2S2]; X-ray Crystal Structures of [Pd3{μ-SNC(Ar′)NS–S,S′}2(PPh3)4] (Ar′ = 4′-C5H4N, 4′-C5H4NBEt3 and 3′-C5H4NBEt3)". European Journal of Inorganic Chemistry 2000, № 5 (2000): 1045–54. http://dx.doi.org/10.1002/(sici)1099-0682(200005)2000:5<1045::aid-ejic1045>3.0.co;2-o.

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41

Banister, Arthur J., Michael I. Hansford, Zdenek V. Hauptman, et al. "Novel S–N ring contractions using the 4-phenyl-1,2,3,5-dithiadiazole dimer, the synthesis and X-ray crystal structures of [(PhCN2S2)2Cl][S3N3], [PhCN2S2][S3N3], and [PhCN2S2][S3N2]Cl, and an ab initio molecular-orbital study of the bonding in [PhCN2S2][S3N3]." J. Chem. Soc., Dalton Trans., no. 9 (1990): 2793–802. http://dx.doi.org/10.1039/dt9900002793.

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42

Deohate, Pradip P., and B. N. Berad. "ChemInform Abstract: Synthesis, Characterization and Antimicrobial Study of Substituted Bis-[1,2,4,5]-dithiadiazine and Bis-[1,3,4]-thiadiazolidine Derivatives." ChemInform 40, no. 19 (2009). http://dx.doi.org/10.1002/chin.200919033.

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Cablewski, Teresa, Craig L. Francis, and Andris J. Liepa. "ChemInform Abstract: N,N-Dialkyl-N′-chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. Part 6. The Preparation of Some Fused [1,4,2,6]Dithiadiazine Dioxides." ChemInform 39, no. 42 (2008). http://dx.doi.org/10.1002/chin.200842155.

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Grekhnev, Dmitriy A., Iuliia V. Novikova, Alena V. Krisanova, et al. "Dithiadiazole derivative 3-(4-nitrophenyl)-5-phenyl-3H-1,2,3,4-dithiadiazole-2-oxide – Novel modulator of store-operated calcium entry." Biochemical and Biophysical Research Communications, August 2022. http://dx.doi.org/10.1016/j.bbrc.2022.08.001.

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SINGH, A. P., R. SINGH, and V. K. VERMA. "ChemInform Abstract: Synthesis of Some 6-Arylamino-3-amino-1,2,4,5-dithiadiazines." ChemInform 20, no. 10 (1989). http://dx.doi.org/10.1002/chin.198910260.

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Novikova, Iuliia V., Dmitriy A. Grekhnev, Arina Oshkolova, et al. "1,2,3,4-dithiadiazole derivatives as a novel class of calcium signaling modulators." Biochemical and Biophysical Research Communications, November 2023, 149333. http://dx.doi.org/10.1016/j.bbrc.2023.149333.

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LENZ, B. G., and B. ZWANENBURG. "ChemInform Abstract: SYNTHESIS OF 1,4,2,5-DITHIADIAZINES, A NEW HETEROCYCLIC SYSTEM, FROM AMINOSULFINES (THIOAMIDE S-OXIDES)." Chemischer Informationsdienst 16, no. 9 (1985). http://dx.doi.org/10.1002/chin.198509264.

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YONEMOTO, K., and I. SHIBUYA. "ChemInform Abstract: Decomposition Reaction of 3-Aryl-6-disubstituted Amino-1,4,2,5-dithiadiazines in the Solid State." ChemInform 20, no. 44 (1989). http://dx.doi.org/10.1002/chin.198944089.

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YONEMOTO, K., I. SHIBUYA, and K. HONDA. "ChemInform Abstract: Formation of 1,4,2,5-Dithiadiazines as a Heterocyclic System by Reaction of 1,4,2-Dithiazolium Salts with Sulfenamides." ChemInform 19, no. 43 (1988). http://dx.doi.org/10.1002/chin.198843121.

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BANISTER, A. J., M. I. HANSFORD, Z. V. HAUPTMAN, S. T. WAIT, and W. CLEGG. "ChemInform Abstract: Direct Insertion of a Nitrogen Atom into the S-S Bond of a 1,2,3,5-Dithiadiazole Ring in a Direct Current Nitrogen Glow Discharge, and X-Ray Crystal Structure of 4-Methyl-1,2,3,5-dithiadiazole." ChemInform 20, no. 49 (1989). http://dx.doi.org/10.1002/chin.198949168.

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