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Journal articles on the topic ']-dithiazolidines'

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Published: 5 June 2025

Last updated: 1 August 2025

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1

N., K. KHANDELWAL, N. BERAD B., and G. PARANJPE M. "Synthesis of 3-t-Butylimino-4-aryl/alkyl-5-aryl/alkylimino-1,2,4-dithiazolidines and their De-t-butylation Into related 3-lmino-1,2,4-dithiazolidines." Journal of Indian Chemical Society Vol. 64, May 1987 (1987): 321–23. https://doi.org/10.5281/zenodo.6236533.

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Department of Chemistry, Nagpur University, Nagpur-440 010 <em>Manuscript received 19 February 1985, revised 8 July 1986, accepted 22 April 1987</em> Synthesis of 3-t-Butylimino-4-aryl/alkyl-5-aryl/alkylimino-1,2,4-dithiazolidines and their De-t-butylation Into related 3-lmino-1,2,4-dithiazolidines

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2

A., P. SINGH, BHATTACHARYA A., SINGH R., and K. VERMA V. "Synthesis and Biological Activity of some 3-Arylimino-5-[2-(6-methyl)benzothiazolyl]-imino-1,2,4-dithiazolidines." Journal of Indian Chemical Society Vol. 68, Aug 1991 (1991): 472–74. https://doi.org/10.5281/zenodo.6196911.

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Department of Applied Chemistry, Institute of Technology, Banaras Hindu University, Varanasi-221 005 <em>Manuscript received 1 February 1991, revised 17 July 1991, accepted 5 August 1991</em> Synthesis and Biological Activity of some 3-Arylimino-5-[2-(6-methyl)benzothiazolyl]-imino-1,2,4-dithiazolidines.

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3

Rai, S. K., Usha K. Tiwari, and P. K. Srivastava. "Synthesis of some 3-(arylimino)-5-(ethylethylidenehydrazido)-1,2,4-dithiazolidines." Journal of Chemical & Engineering Data 30, no. 4 (1985): 515–16. http://dx.doi.org/10.1021/je00042a049.

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4

Poonam, T. Agrawal, and P. Deshmukh Shirish. "Synthesis of new N-lactosylated isodithiobiurets and dithiazolidines (hydrobromide)." Journal of Indian Chemical Society Vol. 86, Jun 2009 (2009): 645–48. https://doi.org/10.5281/zenodo.5811842.

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P. G Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : poonam.agrawal2008 @rediffmail.com <em>Manuscript received 23 May 2008, revised 10 February 2009, accepted 11 February 2009</em> A series of new 1-hepta-<em>O</em>-benzoyl-β-D-lactosyl-5-aryl-2-<em>S-</em>benzyl-2,4-isodithiobiurets and 3-hepta-<em>O</em>-benzoyl-β-D-Iactosylimino-5-arylimino-1,2,4-dithiazolidines (hydrobromide) have been synthesized by the interaction of hepta-<em>O</em>-benzoyl-β-D-lactosyl isothiocyanate with 1-aryl-<em>S</em>-benzyl isothiocarbamides follo

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5

M., G. Dhonde, та P. Deshmukh S. "Synthesis of 3-tetra-O-benzoyl-β-D-glucopyranosylimino-4-phenyl-5-arylimino-1,2,4-dithiazolidines". Journal of Indian Chemical Society Vol. 81, Feb 2004 (2004): 155–56. https://doi.org/10.5281/zenodo.5830183.

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Department of Chemistry, Shri Shivaji College, Akola-444 001, India <em>Manuscript received 31 January 2003, revised 17 July 2003, accepted 11 August 2003</em> Some 3-tetra-<em>O</em>-benzoyl-β-D-glucopyranosylimino-4-phenyl-5-arylimino-1 ,2,4-dithiazolidines (3) have been synthesized for the first time involving interaction of N-tetra-<em>O</em>-benzoyl-β-D-glucopyranosyl-<em>S</em>-chloroisotbiocarbamoyl chloride (1) and 1-phenyl-3-arylthiocarbamides (2).

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6

P., V. Tale, та P. Deshmukh S. "Synthesis of 3-hepta-O-acetyl-β-lactosylimino-4-aryl-5-phenylimino1 ,2,4-dithiazolidines (hydrochlorides)". Journal of Indian Chemical Society Vol. 84, Oct 2007 (2007): 1029–31. https://doi.org/10.5281/zenodo.5827174.

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P. G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em>: prashanttale@rediffmail.com <em>Manuscript received 14 February 2007, revised 10 April 2007, accepted 20 July 2007</em> Some 3-hepta-<em>O</em>-acetyl-β-lactosylimino-4-aryl-5-phenylimino-1,2,4-dithiazolidines (hydrochlorides) (3) have been synthesized for the first time involving interaction of 1-hepta-<em>O</em>-acetyl-β-D-lactosyl-3-aryl thiocarbamnides (1) and <em>N</em>-phenyl-<em>S</em>-chloro isothiocarbomyl chloride (2).

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7

M., G. Dhonde, та P. Deshmukh S. "Synthesis and antimicrobial activity of 4-aryl-5-tetra-O-benzoyl-β-D-glucopyranosylimino- 3-thio-1,2,4-dithiazolidines". Journal of Indian Chemical Society Vol. 84, Jul 2007 (2007): 711–13. https://doi.org/10.5281/zenodo.5824468.

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Shri Mathuradas Mohota College of Science, Urnrer Road, Nagpur-440 009, Maharashtra, India Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : madhudash2001@yahoo.co.in Fax : 91-0724-2450722 <em>Manuscript received 18 May 2005, revised 29 November 2006, accepted 4 May 2007</em> 4-Aryl-5-tetra-<em>O</em>-benzoyl-β-D-glucopyranosylimino-3-thio-1 ,2,4-dithiazolidines have been prepared by the interaction of <em>N</em>-tetra-<em>O</em>-benzoyl-β-D-glucopyranosyi-S-chloro isothiocarbamoyl chloride and ammonium aryl dithiocarbamates. Antimicro

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8

Pradip, P. Deohate, and N. Berad B. "The convenient microwave-assisted synthesis, characterization and structural study of substituted bis-[1,2,4]-dithiazolidines." Journal of Indian Chemical Society Vol. 91, Jul 2014 (2014): 1361–64. https://doi.org/10.5281/zenodo.5726594.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India Department of Chemistry, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440 033, Maharashtra, India <em>E-mail </em>: pradip222091@yahoo.co.in <em>Manuscript received online 05 December 2012, revised 21 February 2014, accepted 28 February 2014</em> A convenient synthesis of substituted bis-[1,2,4]-dithiazolidines has been developed by using the environmentfriendly technique of microwave irradiation. The microwave-assisted synthesis of several members of the titled class

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9

Kavita, M. Heda, та P. Deshmukh Shirish. "Synthesis and biological evaluation of 4-aryl-5-hepta-O-benzoyl-β-D-lactosylimino¬3-hepta-O-benzoyl-β-D-lactosylimino-l,2,4-dithiazolidines (hydrochlorides)". Journal of Indian Chemical Society Vol. 93, Dec 2016 (2016): 1413–16. https://doi.org/10.5281/zenodo.5599109.

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Department of Chemistry, Shri R. L. T. College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : kavitaheda25@gmail.com P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>Manuscript received 04 November 2015, accepted 26 October 2016</em> A series of 4-aryl-5-hepta-<em>O</em>-benzoyl-β-D-lactosylimino-3-hepta-<em>O</em>-benzoyl-β-D-lactosylimino-1,2,4-dithiazolidines (hydrochloride) have been synthesized by the interaction of various 1-hepta-<em>O</em>-benzoyl-β-D-lactosyl-3-aryl thiocarbamides with <em>N</em>-hepta-<em>O</em>

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10

Feng, Yian, Minming Zou, Runjiang Song, Xusheng Shao, Zhong Li, and Xuhong Qian. "Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives." Journal of Organic Chemistry 81, no. 21 (2016): 10321–27. http://dx.doi.org/10.1021/acs.joc.6b01307.

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11

Deohate, Pradip P., and B. N. Berad. "ChemInform Abstract: The Convenient Microwave-Assisted Synthesis, Characterization and Structural Study of Substituted Bis-[1,2,4]-dithiazolidines." ChemInform 46, no. 9 (2015): no. http://dx.doi.org/10.1002/chin.201509175.

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12

Quraishi, M. A., and R. Sardar. "Dithiazolidines—A New Class of Heterocyclic Inhibitors for Prevention of Mild Steel Corrosion in Hydrochloric Acid Solution." CORROSION 58, no. 2 (2002): 103–7. http://dx.doi.org/10.5006/1.3277308.

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13

Gharad, Spruha A., Baliram N. Berad, and Snehal A. Chavan. "Synthesis of quinoline based [1,2,4]-dithiazolidines through sulfur-sulfur bond formation and their evaluation as anti-inflammatory and antibacterial agents." Phosphorus, Sulfur, and Silicon and the Related Elements 191, no. 2 (2016): 254–58. http://dx.doi.org/10.1080/10426507.2015.1100179.

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14

Ansari, Monish A., Dhananjay Yadav, Sonam Soni, Abhijeet Srivastava та Maya Shankar Singh. "Visible-Light-Mediated Synthesis of 1,2,4-Dithiazolidines from β-Ketothioamides through a Hydrogen-Atom-Transfer Photocatalytic Approach of Eosin Y". Journal of Organic Chemistry 84, № 9 (2019): 5404–12. http://dx.doi.org/10.1021/acs.joc.9b00406.

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15

Dhonde, Madhukar G., та Shirish P. Deshmukh. "Synthesis and Antimicrobial Activity of 4‐Aryl‐5‐phenyl‐imino‐3‐(tetra‐O‐benzoyl‐β‐D‐glucopyranosylimino)‐1,2,4‐dithiazolidines (Hydrochlorides)". Journal of Carbohydrate Chemistry 23, № 5 (2004): 305–11. http://dx.doi.org/10.1081/car-200030097.

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16

Hardas, Aruna, and Priti Tayade (Gosavi). "Synthesis and Schematic Mechanism of 3-Phenylamino-4-phenyl-5-tetra-O-acetyl-b-Dglucopyranosylimino- 1,2,4-dithiazolidines and Its De-acetylated Nucleoside." Asian Journal of Chemistry 30, no. 10 (2018): 2310–16. http://dx.doi.org/10.14233/ajchem.2018.21472.

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17

An, Zhenyu, Ting Wang, Yafeng Liu, Yi Ren, and Rulong Yan. "A catalyst-free method for the synthesis of 1,4,2-dithiazoles from isothiocyanates and hydroxylamine triflic acid salts." Organic & Biomolecular Chemistry 19, no. 28 (2021): 6206–9. http://dx.doi.org/10.1039/d1ob00938a.

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18

TITTELBACH, F., and A. SCHELLHAAS. "ChemInform Abstract: Cycloaddition Elimination Reactions of Phenyl Isocyanate with Oxo and Thiono Derivatives of 5-Imino-1,2,4-dithiazolidines and 3-Thiono-1,2,4- thiadiazolidines with Aliphatic Substitution (Mustard Oil Oxides and Sulfides)." ChemInform 25, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199406148.

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19

Wood, Mark E., Daniel J. Cane-Honeysett, Michael D. Dowle, Simon J. Coles, and Michael B. Hursthouse. "Synthetic and structural studies on 1,2,4-dithiazolidine-3,5-dione derivatives." Organic & Biomolecular Chemistry 1, no. 17 (2003): 3015. http://dx.doi.org/10.1039/b305096c.

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20

Chen, Lin, Tracy R. Thompson, Robert P. Hammer, and George Barany. "Synthetic, Mechanistic, and Structural Studies Related to 1,2,4-Dithiazolidine-3,5-dione." Journal of Organic Chemistry 61, no. 19 (1996): 6639–45. http://dx.doi.org/10.1021/jo960723u.

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21

Cane-Honeysett, Daniel J., Michael D. Dowle, and Mark E. Wood. "ChemInform Abstract: 1,2,4-Dithiazolidine-3,5-dione: A Nucleophilic Isocyanate “Building Block”." ChemInform 32, no. 8 (2001): no. http://dx.doi.org/10.1002/chin.200108157.

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22

Ponomarov, Oleksandr, Zdeňka Padělková, and Jiří Hanusek. "Mechanism of sulfur transfer from 1,2,4-dithiazolidine-3,5-diones to triphenylphosphines." Journal of Physical Organic Chemistry 26, no. 7 (2013): 560–64. http://dx.doi.org/10.1002/poc.3131.

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23

Wood, Mark E., Daniel J. Cane-Honeysett, and Michael D. Dowle. "1,2,4-Dithiazolidine-3,5-dione as an isocyanate equivalent in the Mitsunobu reaction." Journal of the Chemical Society, Perkin Transactions 1, no. 18 (August 19, 2002): 2046–47. http://dx.doi.org/10.1039/b206793e.

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24

S., K. Deshmukh, T. Agrawal P., and P. Deshmukh S. "Synthesis and antimicrobial activity of some new lactosylated-1 ,2,4-dithiazolidine (hydrochlorides)." Journal of Indian Chemical Society Vol. 88, Nov 2011 (2011): 1759–62. https://doi.org/10.5281/zenodo.5791770.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India P. G. Department of Chemistry, Shri R. L. T. College of Science, Akola, Maharashtra, India <em>Manuscript received 06 October 2009, revised 23 February 2011, accepted 25 April 2011</em> Several 3-hepta-0-benzoyl-P-n-lactosylimino-4-aryl-5-phenylimino and 4-phenyl-5-hepta-0-acetyi-P-DIactosylimino-3-arylimino-1,2,4-dithiazolidine (hydrochlorides) have been prepared by the interaction of 1-hepta-0-benzoyi-β-D-lactosyl-3-aryl thiocarbamides and <em>N</em>-phenyl-<em>S</em>-chloro isothiocarbamoyl chloride a

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25

Deshmukh, S. K., P. T. Agrawal, and S. P. Deshmukh. "ChemInform Abstract: Synthesis and Antimicrobial Activity of Some New Lactosylated-1,2,4-dithiazolidine (Hydrochlorides)." ChemInform 43, no. 41 (2012): no. http://dx.doi.org/10.1002/chin.201241142.

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26

CHEN, L., T. R. THOMPSON, R. P. HAMMER, and G. BARANY. "ChemInform Abstract: Synthetic, Mechanistic, and Structural Studies Related to 1,2,4- Dithiazolidine-3,5-dione (IV)." ChemInform 28, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199705166.

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27

Wood, Mark E., Victoria M. Annis, and Clifford D. Jones. "Unusual reactivity of N-acyl imides: N-aroyl-1,2,4-dithiazolidine-3,5-diones as acyl isocyanate equivalents." Organic & Biomolecular Chemistry 6, no. 22 (2008): 4099. http://dx.doi.org/10.1039/b814677b.

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28

Chibale, Kelly, and Richard Gessner. "A New and Simple Synthesis of Sulfonyl Ureas from Sulfonamides and N-Alkyl-1,2,4-dithiazolidine-3,5-diones." Synlett 2009, no. 17 (2009): 2839–43. http://dx.doi.org/10.1055/s-0029-1217960.

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29

Barany, Michael J., Robert P. Hammer, R. B. Merrifield, and George Barany. "Efficient Synthesis of 1,2,4-Dithiazolidine-3,5-diones [Dithiasuccinoyl-Amines] from Bis(chlorocarbonyl)disulfane Plus Bis(trimethylsilyl)amines." Journal of the American Chemical Society 127, no. 2 (2005): 508–9. http://dx.doi.org/10.1021/ja0455446.

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30

BRIEL, D., and S. LEISTNER. "ChemInform Abstract: Investigations Towards the Synthesis of 6,6′-(1,2,4-Dithiazolidine-3,5- ylidene)-bis-2,4-cyclohexadien-1-ones." ChemInform 25, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199431149.

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31

TITTELBACH, F. "ChemInform Abstract: Synthesis and Dimroth Isomerization of Disubstituted 5-Imino-1,2,4- dithiazolidine-3-thiones (Mustard Oil Sulfides)." ChemInform 22, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199138169.

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32

Xu, Q., K. Musier-Forsyth, R. P. Hammer, and G. Barany. "Use of 1,2,4-Dithiazolidine-3,5-Dione (DtsNH) and 3-Ethoxy-1,2,4-Dithiazoline-5-One (EDITH) for Synthesis of Phosphorothioate-Containing Oligodeoxyribonucleotides." Nucleic Acids Research 24, no. 9 (1996): 1602–7. http://dx.doi.org/10.1093/nar/24.9.1602.

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33

Barany, George, Doyle Britton, Lin Chen, et al. "Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach–Weiss–Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones." Journal of Organic Chemistry 80, no. 22 (2015): 11313–21. http://dx.doi.org/10.1021/acs.joc.5b01826.

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34

Kuriyama, Mineo, Noritake Yasuoka, Nobutami Kasai, Mitsuo Komatsu, Yoshiki Ohshiro, and Toshio Agawa. "The Crystal and Molecular Structures of 4-Ethyl-3,5-bis(phenylimino)-1,2,4-dithiazolidine and 2-Ethyl-4-phenyl-5-phenylimino-1,2,4-thiadiazolidin-3-thione." Bulletin of the Chemical Society of Japan 59, no. 4 (1986): 987–91. http://dx.doi.org/10.1246/bcsj.59.987.

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35

Tittelbach, Franz, and A. Schellhaas. "Cycloadditions-Eliminierungsreaktionen von Phenylisocyanat mit Oxo-und Thionoderivaten aliphatisch substituierter 5-Imino-1,2,4-dithiazolidine und 3-Thiono-1,2,4-thiadiazolidine (Senf�loxide und Senf�lsulfide)." Journal f�r Praktische Chemie/Chemiker-Zeitung 334, no. 8 (1992): 685–90. http://dx.doi.org/10.1002/prac.19923340808.

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36

Boese, Roland, Heinz Oberhammer, Peter Pulay, and Alfred Waterfeld. "Structure and conformation of 4,4,5,5-tetrafluoro-1,3,2-dithiazolidine, cyclo-S-NH-S-CF2-CF2: a gas electron diffraction, x-ray diffraction, and ab initio study." Journal of Physical Chemistry 97, no. 38 (1993): 9625–29. http://dx.doi.org/10.1021/j100140a017.

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37

Brooks, Wendell V. F., Scott Brownridge, Jack Passmore, Melbourne J. Schriver, and Xiaoping Sun. "Preparation and characterization of 1,3,2-dithiazolidine and 1,4-dithia-7-azabicyclo[2.2.1]heptane cations, and a mechanistic study of the cycloaddition reactions of alkenes with SNS." Journal of the Chemical Society, Dalton Transactions, no. 9 (1996): 1997. http://dx.doi.org/10.1039/dt9960001997.

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38

BOESE, R., H. OBERHAMMER, P. PULAY, and A. WATERFELD. "ChemInform Abstract: Structure and Conformation of 4,4,5,5-Tetrafluoro-1,3,2-dithiazolidine, Cyclic S-NH-S-CF2-CF2. A Gas Electron Diffraction, X-Ray Diffraction, and ab initio Study." ChemInform 25, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199402037.

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39

SINGH, A. P., A. BHATTACHARYA, and V. K. VERMA. "ChemInform Abstract: Synthesis of 5-Substituted Benzothiazolylimino-3-arylimino-1,2,4-dithiazolidines." ChemInform 21, no. 48 (1990). http://dx.doi.org/10.1002/chin.199048161.

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40

SINGH, A. P., M. R. ALI, R. SINGH, and V. K. VERMA. "ChemInform Abstract: Synthesis of 5-(N-Cyclohexylidenehydrazono)-3-arylimino-1,2,4-dithiazolidines." ChemInform 21, no. 48 (1990). http://dx.doi.org/10.1002/chin.199048164.

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41

RAI, S. K., U. K. TIWARI, and P. K. SRIVASTAVA. "ChemInform Abstract: Synthesis of Some 3-(Arylimino)-5-(ethylethylidenehydrazido)-1,2,4-dithiazolidines." Chemischer Informationsdienst 17, no. 6 (1986). http://dx.doi.org/10.1002/chin.198606164.

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42

KHANDELWAL, N. K., B. N. BERAD, and M. G. PARANJPE. "ChemInform Abstract: Synthesis of 3-tert-Butylimino-4-aryl/alkyl-5-aryl/alkylimino-1,2,4-dithiazolidines and Their De-tert-butylation into Related 3-Imino-1,2,4- dithiazolidines." ChemInform 19, no. 7 (1988). http://dx.doi.org/10.1002/chin.198807177.

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43

Agrawal, Poonam T., and Shirish P. Deshmukh. "ChemInform Abstract: Synthesis of New N-Lactosylated Isodithiobiurets (III) and Dithiazolidines (IV) (Hydrobromide)." ChemInform 41, no. 19 (2010). http://dx.doi.org/10.1002/chin.201019187.

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44

Dhonde, M. G., and S. P. Deshmukh. "Synthesis of 3-Tetra-O-benzoyl-?-D-glucopyranosylimino-4-phenyl-5-arylimino-1,2, 4-dithiazolidines." ChemInform 36, no. 3 (2005). http://dx.doi.org/10.1002/chin.200503191.

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45

Manna, Paresh, R. Singh, K. K. Narang, and S. K. Manna. "Synthesis, Antifungal, Antitumor and Antiinflammatory Activities of Some New 5-Substituted Arylimino-3-(2,4-diethoxyarylimino)-1,2,4-dithiazolidines." ChemInform 37, no. 1 (2006). http://dx.doi.org/10.1002/chin.200601153.

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46

Dhonde, Madhukar G., та Shirish P. Deshmukh. "Synthesis and Antimicrobial Activity of 4-Aryl-5-phenyl-imino-3- (tetra-O-benzoyl-β-D-glucopyranosylimino)-1,2,4-dithiazolidines (Hydrochlorides)." ChemInform 36, № 33 (2005). http://dx.doi.org/10.1002/chin.200533250.

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47

"1,2,4-Dithiazolidine-3,5-dione: A Nucleophilic Isocyanate "Building Block"." Synlett 2000, no. 11 (2000): 1622–24. http://dx.doi.org/10.1055/s-2000-7934.

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48

Wood, Mark E., Daniel J. Cane-Honeysett, Michael D. Dowle, Simon J. Coles, and Michael B. Hursthouse. "Synthetic and Structural Studies on 1,2,4-Dithiazolidine-3,5-dione Derivatives." ChemInform 35, no. 1 (2004). http://dx.doi.org/10.1002/chin.200401114.

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49

Wood, Mark E., Daniel J. Cane-Honeysett, and Michael D. Dowle. "1,2,4-Dithiazolidine-3,5-dione as an Isocyanate Equivalent in the Mitsunobu Reaction." ChemInform 34, no. 8 (2003). http://dx.doi.org/10.1002/chin.200308123.

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Wood, Mark E., Victoria M. Annis, and Clifford D. Jones. "ChemInform Abstract: Unusual Reactivity of N-Acyl Imides: N-Aroyl-1,2,4-dithiazolidine-3,5-diones as Acyl Isocyanate Equivalents." ChemInform 40, no. 13 (2009). http://dx.doi.org/10.1002/chin.200913080.

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