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Journal articles on the topic 'Thiocarbamides'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

P. L. Harale, M. E. Shelke, D.T. Tayade, and A. R. Kurhe. "Synthesis of 3-(substitutedthiocarbamide)-aniline derivatives from di-tert-butyl dicarbonate (BoC) protected 3-chloroaniline." GSC Biological and Pharmaceutical Sciences 28, no. 3 (2024): 046–52. http://dx.doi.org/10.30574/gscbps.2024.28.3.0313.

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Synthesis of substituted thiocarbamide derivatives is important in the fields of medicinal, agricultural, chemical, and pharmaceutical. Thiocarbamides are commonly utilized as starting materials for several organic synthetic processes and have been studied in search for easy and effective methods of chemical synthesis. In the existing research work, 3-chloroaniline was protected by a di-tert-butyl dicarbonate (BoC) protecting agent. Substituted thiocarbamide derivatives were synthesized using condensation of various substituted thioureas with amino group-protected 3-chloroaniline. The structur

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2

P., L. Harale, E. Shelke M., Tayade D.T., and R. Kurhe A. "Synthesis of 3-(substitutedthiocarbamide)-aniline derivatives from di-tert-butyl dicarbonate (BoC) protected 3-chloroaniline." GSC Biological and Pharmaceutical Sciences 28, no. 3 (2024): 046–52. https://doi.org/10.5281/zenodo.14709141.

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Synthesis of substituted thiocarbamide derivatives is important in the fields of medicinal, agricultural, chemical, and pharmaceutical. Thiocarbamides are commonly utilized as starting materials for several organic synthetic processes and have been studied in search for easy and effective methods of chemical synthesis. In the existing research work, 3-chloroaniline was protected by a di-tert-butyl dicarbonate (BoC) protecting agent. Substituted thiocarbamide derivatives were synthesized using condensation of various substituted thioureas with amino group-protected 3-chloroaniline. The structur

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3

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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4

Prashant, R. Mahalle, V. Korpe Gajanan, and P. Deshmukh Shirish. "New N-galactosides : Synthesis of N-galactosylated thiocarbamides, benzothiazolyl thiocarbamides and thiocarbamates." Journal of Indian Chemical Society Vol. 85, Sep 2008 (2008): 953–58. https://doi.org/10.5281/zenodo.5820384.

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P.G Department ofChemisty, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail:</em> prmahalle@rediffmail.com <em>Manuscript received 22 August 2007, revised 22 May 2008, accepted 3 June 2008</em> The title compounds were prepared by the condensation of tetra-<em>O</em>-acetyi-β-D-galactopyranosyl isothiocyanate with several amines, 2-aminobenzothiazole/substituted benzothiazoles and alcohols respectively. The structure of these new <em>N</em>-galactoside has been established on the basis of usual chemical transformations and IR, NMR and Mass spectral studies of some typica

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5

M., T. Sangole, and P. Deshmukh S. "Synthesis and antimicrobial activity of novel N-maltosylated thiocarbamides, benzothiazolyl thiocarbamides and thiocarbamates." Journal of Indian Chemical Society Vol. 89, May 2012 (2012): 689–94. https://doi.org/10.5281/zenodo.5763480.

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P. G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : mamtasangole@rediffmail.com <em>Manuscript received 16 March 2009. revised 07 October 2010, accepted 19 September 2011</em> A new class of <em>N</em>-maltosides has been investigated in which maltosyl isothiocyanate was readily transformed into corresponding l-hepta-<em>O</em>-bcnzoyi-β-D-maltosyl-3-aryl thiocarbamides, 1-hepta-<em>O</em>-benzoyl-β-D-maltosyl-3-substituted benzothiazolyl thiocarbamides and 1-hepta-<em>O</em>-benzoyl-β-D-maltosyl-0-alkyl thiocarbamates on reac

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6

Tayade, D. T., and A. A. Dhande. "Novel Synthesis of Norepinephrine Thiocarbamides." Asian Journal of Research in Chemistry 11, no. 4 (2018): 710. http://dx.doi.org/10.5958/0974-4150.2018.00125.6.

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7

Ramadas, Krishnamurthy, and Natarajan Srinivasan. "A Convenient Route to Substituted Thiocarbamides." Synthetic Communications 25, no. 21 (1995): 3381–87. http://dx.doi.org/10.1080/00397919508013859.

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8

Potikha, L. M., та V. A. Kovtunenko. "Reaction of γ-bromodipnone with thiocarbamides". Chemistry of Heterocyclic Compounds 43, № 4 (2007): 521–22. http://dx.doi.org/10.1007/s10593-007-0082-1.

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9

S., P. DESHMUKH, and G. PARANJPE M. "Synthesis of N-Glucopyranosyl Benzothiazolyl Thiocarbamides." Journal of Indian Chemical Society Vol. 62, May 1985 (1985): 375–76. https://doi.org/10.5281/zenodo.6302905.

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Department of Chemistry, Nagpur University, Nagpur-440 010 <em>Manuscript received 18 September 1984, revised 5 February 1985, accepted 29 April 1985</em> 1-Tetra-<em>O</em>-acetyl-<em>β</em>-D-glucopyranosyl-3-substituted-benzothiazolyl thiocarbamides (3) have been prepared by the interaction of tetra-<em>O</em>-acetyl-<em>β</em>-D-glueopyranosyl isothiocyanate and 2-aminobenzothiazole/substituted-benzothiazoles.

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10

P., S. MITTAL, KUMAR NARINDER, and D. TANEJA A. "Synthesis of some Carboxyalkyl- and Pyrimidyl-substituted-thiocarbamides as Potential Fungicides and Nematicides." Journal of Indian Chemical Society Vol. 65, May 1988 (1988): 382–84. https://doi.org/10.5281/zenodo.6298880.

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D. N. College, Hisar Department of Plant Breeding, Haryana Agricultural University, Hisar-125 004 <em>Manuscript received 1 April 1987, revised 8 February 1988, accepted 11 March 1988</em> Synthesis of some Carboxyalkyl- and Pyrimidyl-substituted-thiocarbamides as Potential Fungicides and Nematicides.

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11

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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12

V. Yadgire, Atul, Gajanan V. Korpe, and Shirish P. Deshmukh. "Comparative Study of Microwave Induced and Conventional Synthesis of Acetylated Sugar Isothiocyanates and Related Thiocarbamides." E-Journal of Chemistry 8, no. 4 (2011): 1614–19. http://dx.doi.org/10.1155/2011/473646.

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The synthesis of several acetylated sugar isothiocyanates have been carried out under microwave irradiation in excellent yields of products by using related bromides and lead thiocyanate in sodium dried xylene. Several acetylated sugar thiocarbamides have been synthesized by the interaction of respective acetylated sugar isothiocyanates with appropriate aryl amines under microwave irradiation.

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13

Pawar, Swati. "Synthesis and Antithyroidal Evaluation of N–Aryl Formamidino–N–(Substituted) Aryl Thiocarbamides." International Journal of Advance Research and Innovation 2, no. 1 (2014): 25–35. http://dx.doi.org/10.51976/ijari.211404.

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Several N–aryl formamidino derivatives of thiocarbamides were synthesized. The structure and purity of the prepared compounds were characterized by elemental, spectral (IR) and TLC analysis. These molecules were evaluated for their efficacy as antithyroidals by radioactive iodine uptake method the activity (Potency) of synthesized compounds were compared with standard drug Thiouracil.

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14

Doerge, Daniel R. "Hydroperoxide-Dependent Metabolism of Goitrogenic Thiocarbamides by Lactoperoxidase." Xenobiotica 18, no. 11 (1988): 1291–96. http://dx.doi.org/10.3109/00498258809042252.

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15

RAMADAS, K., and N. SRINIVASAN. "ChemInform Abstract: A Convenient Route to Substituted Thiocarbamides." ChemInform 27, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199603081.

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16

M., Zahurul Haque, Omar Faruq M., and Umar Ali M. "Synthesis of some new thiocarbamides from a constituent of lac and studies on their antimicrobial activities." Journal of Indian Chemical Society Vol. 79, Oct 2002 (2002): 841–42. https://doi.org/10.5281/zenodo.5847960.

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BCSIR Laboratories, Rajshahi, Bangladesh <em>E-mail : </em>bcsirraj @librabd.net Department of Chemistry, Rajshahi University, Rajshahi, Bangladesh <em>Manuscript received 21 May 2001, revised 14 February 2002, accepted 24 April 2002</em> Some new thiocarbamides have been synthesized by the reaction of aleurityl hydrazide (prepared from aleuritic acid isolated from Bangladeshi lac) with different isothiocyanates. Antibacterial activities of the compounds have been determined and most of them are found highly active.

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17

A., D. NAKRANI, V. RATHOD B., and J. SHAH K. "Manganese(II) Complexes of N-Phenyl-N'-(6-substituted)benzothiazolylthiocarbamide." Journal of Indian Chemical Society Vol. 68, Sep 1991 (1991): 517–18. https://doi.org/10.5281/zenodo.6153897.

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University Department of Chemistry, Bhavnagar University, Bhavnagar-364-002 Manuscript received 27 May 1991, accepted 3 September 1991 Manganese(II) Complexes of <em>N</em>-Phenyl-<em>N'</em>-(6-substituted)benzothiazolylthiocarbamide.

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18

Talekar, P. R. "Effects on Germination Pattern of Jowar of Novel Synthesis of N-Substituted thioamidodicyandiamide." International Journal of Advance and Applied Research 5, no. 23 (2024): 121–26. https://doi.org/10.5281/zenodo.13621901.

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Abstract:  Plant physiology has increasingly important role in agricultural research problem. One of the primary tasks in the future will be to increase production of food and resist pathogen of the crop. Organic drugs have intense biological activity to the seed before sowing in order to control and suppress the pathogens. So the aim of the present work is to study the above said topic. In the present work in our laboratory novel series of 1-[S-TAG-N substituted thioamido] dicyandiamide have been synthesized successfully by refluxing TAG Br with cyanoamidino substituted thiocarbamid

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19

Ellis, Carol A., Michael A. Miller, James Spencer, Julio Zukerman-Schpector, and Edward R. T. Tiekink. "Co-crystallization experiments of thiocarbamides with bipyridine-type molecules." CrystEngComm 11, no. 7 (2009): 1352. http://dx.doi.org/10.1039/b822555a.

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20

Siddharth. A. Waghmare and Kuldip U. Dongare. "Design, synthesis, and spectral characterization of series of thiocarbamides with coumarin backbone." International Journal of Science and Research Archive 10, no. 2 (2023): 855–59. http://dx.doi.org/10.30574/ijsra.2023.10.2.1035.

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Recently a series of 7-(3-thiocarbamido), 7-(3-phenylthiocarbamido), 7-(3-(1,3-dimethyl) thiocarbamido), 7-(3-methylthiocarbamido), 7-(3-allylthiocarbamido)-4-methyl-2H-chromen-2-one (IIIa-e) had been synthesized by refluxing 7-chloro-4-methyl-2H-chromen-2-one (I) with thiourea, N-phenylthiourea, 1,3-dimethylthiourea, N-methylthiourea and N-allylthiourea (IIa-e) in isopropanol medium in 1:1 molar proportion for 5 hours. All the synthesized compounds structures were justified on the basis of chemical tests, elemental study and spectral characterization.

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21

Yadava, B. P., and B. Singh. "The powder X-ray diffraction studies of some substituted thiocarbamides." Crystal Research and Technology 25, no. 10 (1990): K245—K248. http://dx.doi.org/10.1002/crat.2170251026.

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22

NARINDER, KUMAR, D. TANEJA A., and P. KUDESIA V. "Effect of Solvents on the Spectra of Carboxyalkyl and Thiazolyl Substituted Thiocarbamides." Journal of Indian Chemical Society Vol. 65, Jan 1988 (1988): 40–43. https://doi.org/10.5281/zenodo.6010506.

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Department of Chemistry, D. N. College, Hisar-125 001 Department of Plant Breeding, Haryana Agricultural University, Hisar-125 004 D. N. (P. G.) College, Meerut <em>Manuscript received 30 June 1981, accepted 4 November 1981</em> Electronic absorption spectra of twenty one carboxyalkyl and thiazolyl substituted thiocarbamides have been examined in a series of solvents covering a broad polarity range i.e. from chloroform (Z 63 2) to methanol (Z 83.6). Transition energies were calculated and plotted against Z-values, a new empirical measurement of solvent polarity A linear rel

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23

Gauravkumar, S. Patkar, S. Zade Varsha, and V. Korpe Gajanan. "Versatile synthesis of N-substituted lactopyranosyl formamidines by desulfurization of the corresponding thiocarbamides." Journal of Indian Chemical Society Vol. 92, Mar 2015 (2015): 393–97. https://doi.org/10.5281/zenodo.5678814.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 003, Maharashtra, India <em>E-mail</em> : g_korpe@rediffmail.com, korpegv@rediffmail.com <em>Manuscript received online 16 August 2014, accepted 18 September 2014</em> 1-Hepta-<em>O</em>-acetyl-β-D-lactopyranosyl-3-<em>H</em>/aryl formamidines were easily synthesized by desulfurization of 1- hepta-<em>O</em>-acetyl-β-D-lactopyranosyl-<em>H</em>/aryl thiocarbamides with Raney nickel. From the synthetic point of view, the protocol can be considered and efficient for the synthesis of lactosylated formamidines in moderate to e

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24

Sangeeta, Mehrotra, Pandey Vaishali, Lakhan Ram, and K. Srivastava P. "Synthesis and antibacterial activities of 1-(p-chloropheny1)- 2-amino/hydrazino-4-nitrophenyl/p-chloropheny1)-1,6-dihydro ¬1,3,5-triazine-6-thiones and related thiocarbamides, thiosemicar- bazides and Schiff bases." Journal of Indian Chemical Society Vol. 79, Feb 2002 (2002): 176–78. https://doi.org/10.5281/zenodo.5873172.

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Department of Chemistry, Banaras Hindu University, Varanasi-221 005, India  <em>Fax : </em>91-542-368174 <em>Manuscript received 27 November 2000, revised 19 March 2001. accepted 5 June 2001</em> 1-(p-ChlorophenyI)-2-benzylmercapto-4-0-nitrophenyl/p-chloropheny1)-1,6-dihydro-1,3,5-trazine-6-thiones (1) on treatment with ammonia/hydrazine hydrate under suitable conditions afford the corresponding 2-amino/hydrazino derivatives (2, 3). The latter on treatment with aryl isothiocyanates/aryl aldehydes afford the related thiocarbamides/thiosemicarbazides/Schiff bases (4.6) which have been

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25

A., RAMESH, KRISHNAMACHARYULU J., K. RAVINDRANATH L., and BRAHMAJI RAO S. "Electrochemical Behaviour of Substituted-N-aryl-N1-2-( 4-p-anisyl-5-arylazothiazolyl)thiocarbamides." Journal of Indian Chemical Society Vol. 68, Oct 1991 (1991): 545–48. https://doi.org/10.5281/zenodo.5969635.

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Department of Chemistry, J.N.T.U. College of Engineering, Anantapnr-515 002 Department of Chemistry, S. K. University, Anantapur-515 003 <em>Manuscript received 30 March 1990, revised 26 August 1991, accepted 20 September 1991</em> <em>N</em>-Aryl-<em>N</em><sup>1</sup>-2 (4-<em>p</em>-anisyl-5- arylazothiazolyl)thiocarbamides (1-5) exhibit a well-defined reduction wave at DME and a cathodic peak at HMDE in Britton-Robinson butlers (pH 20 -10.0) containing 60% (v/v) dimethylformamide. The products of electrolysis have been characterised and a plausible mechanism has been suggested.

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26

P., S. MITTAL, KUMAR NARINDER, S. TYAGI J., and D. TANEJA A. "Effect of Solvents of different Polarities on the Spectra of some Carboxyalkylthiocarbamides." Journal of Indian Chemical Society Vol. 65, Dec 1988 (1988): 874–76. https://doi.org/10.5281/zenodo.6104813.

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Department of Chemistry, D. N. College, Hisar-125 001 Meerut College, Meerut Department of Plant Breeding, Haryana Agricultural University, Hisar-125 004 <em>Manuscript received 24 February 1988, revised 1 August 1988, accepted 1 September 1988</em> Effect of Solvents of different Polarities on the Spectra of some Carboxyalkylthiocarbamides.

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27

S. Kadu, Samidha, and G. V. Korpe. "NOVEL SYNTHESIS AND CHARACTERISATION OF SOME BENZYLIDENE DERIVATIVES OF GLYCOSYL THIOCARBAMIDES." Rasayan Journal of Chemistry 12, no. 03 (2019): 1058–62. http://dx.doi.org/10.31788/rjc.2019.1235128.

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28

Vlasova, N. N., O. Yu Grigor’eva, E. N. Oborina, Yu N. Pozhidaev, and M. G. Voronkov. "Reaction of dioxides derived from organosilicon thiocarbamides with ammonia and methylamine." Russian Journal of General Chemistry 76, no. 12 (2006): 1870–73. http://dx.doi.org/10.1134/s107036320612005x.

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29

Samidha, S. Kadu, V. Korpe Gajanan, and P. Karyakarte R. "Novel synthesis of some N-glycosyl benzimidazolyl thiocarbamides and their antimicrobial activity." Journal of Indian Chemical Society Vol. 93, Dec 2016 (2016): 1389–92. https://doi.org/10.5281/zenodo.5598963.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : samidhakadu@gmail.com Department of Microbiology, Govt. Medical College, Akola-444 001, Maharashtra, India <em>Manuscript received online 25 July 2015, accepted 09 August 2016</em> Several 1-peracetyl and perbenzoyl glycosyl benzimidazolyl thiocarbamides were synthesized by the interaction of peracetyl and perbenzoyl glycosyl isothiocyanate and 2-amino benzimidazole. The identities of these newly synthesized compounds were established on the basis of usual chemical transformations and IR, <s

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Decker, Caroline J., and Daniel R. Doerge. "Covalent binding of 14C- and 35S-labeled thiocarbamides in rat hepatic microsomes." Biochemical Pharmacology 43, no. 4 (1992): 881–88. http://dx.doi.org/10.1016/0006-2952(92)90256-i.

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31

Kim, Young Mi, and Daniel M. Ziegler. "Size Limits of Thiocarbamides Accepted as Substrates by Human Flavin-Containing Monooxygenase 1." Drug Metabolism and Disposition 28, no. 8 (2000): 1003–6. https://doi.org/10.1016/s0090-9556(24)15176-8.

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32

Chigwada, Tabitha R., and Reuben H. Simoyi. "S-Oxygenation of Thiocarbamides II: Oxidation of Trimethylthiourea by Chlorite and Chlorine Dioxide." Journal of Physical Chemistry A 109, no. 6 (2005): 1094–104. http://dx.doi.org/10.1021/jp045650u.

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Chigwada, Tabitha R., Edward Chikwana, and Reuben H. Simoyi. "S-Oxygenation of Thiocarbamides I: Oxidation of Phenylthiourea by Chlorite in Acidic Media." Journal of Physical Chemistry A 109, no. 6 (2005): 1081–93. http://dx.doi.org/10.1021/jp0458654.

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Guo, Wei-Xi A., Lawrence L. Poulsen, and Daniel M. Ziegler. "Use of thiocarbamides as selective substrate probes for isoforms of flavin-containing monooxygenases." Biochemical Pharmacology 44, no. 10 (1992): 2029–37. http://dx.doi.org/10.1016/0006-2952(92)90106-s.

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35

Motohashi, Noriko, and Itsuhiko Mori. "Thiol-induced hydroxyl radical formation and scavenger effect of thiocarbamides on hydroxyl radicals." Journal of Inorganic Biochemistry 26, no. 3 (1986): 205–12. http://dx.doi.org/10.1016/0162-0134(86)80042-3.

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Watson, D. G., C. D. Bates, G. G. Skellern, R. Mairs, S. Martin, and C. J. W. Brooks. "The analysis of thiocarbamides by gas chromatography/negative-ion chemical-ionization mass spectrometry." Rapid Communications in Mass Spectrometry 5, no. 3 (1991): 141–42. http://dx.doi.org/10.1002/rcm.1290050311.

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Chigwada, Tabitha, Wilbes Mbiya, Kudzanai Chipiso, and Reuben H. Simoyi. "S-Oxygenation of Thiocarbamides V: Oxidation of Tetramethylthiourea by Chlorite in Slightly Acidic Media." Journal of Physical Chemistry A 118, no. 31 (2014): 5903–14. http://dx.doi.org/10.1021/jp504018k.

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38

CHANDE, M. S., та N. M. PAINGANKAR. "ChemInform Abstract: Investigations on the Reaction of α,α- Dibromodiethylmalonate with Thiocarbamides. Part 1." ChemInform 26, № 17 (2010): no. http://dx.doi.org/10.1002/chin.199517034.

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Akhmedov, R. Yu, I. A. Rzaeva, V. M. Farzaliev, and M. A. Allakhverdiev. "The synthesis of some 3-thietanyl-substituted thiocarbamides and the study of their antioxidant activity." Petroleum Chemistry 49, no. 5 (2009): 427–31. http://dx.doi.org/10.1134/s096554410905017x.

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40

Chigwada, Tabitha R., Edward Chikwana, Tinashe Ruwona, Olufunke Olagunju, and Reuben H. Simoyi. "S-Oxygenation of Thiocarbamides. 3. Nonlinear Kinetics in the Oxidation of Trimethylthiourea by Acidic Bromate†." Journal of Physical Chemistry A 111, no. 45 (2007): 11552–61. http://dx.doi.org/10.1021/jp074897z.

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Patkar, Gauravkumar S., Varsha S. Zade, and Gajanan V. Korpe. "ChemInform Abstract: Versatile Synthesis of N-Substituted Lactopyranosil Formamides by Desulfurization of the Corresponding Thiocarbamides." ChemInform 46, no. 42 (2015): no. http://dx.doi.org/10.1002/chin.201542204.

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42

S., S. Ubarhande, G. Thakare V., and N. Berad B. "Microwave induced improved synthesis of monoaryl thiocarbamides, 1,3-diarylthiocarbamides, 1,3-diarylcarbamides and monoaryl-2,4-dithiobiurets." Journal of Indian Chemical Society Vol. 87, Sep 2010 (2010): 1137–41. https://doi.org/10.5281/zenodo.5804801.

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P.G. Department of Chemistry, Shri Shivaji Science College, Amravati-444 603, Maharashtra, India <em>E-mail:</em> shri_orgchem@rediffmail.com Department of Chemistry, Rastrasant Tukodoji Maharaj Nagpur University, Nagpur-440 010, Maharashtra, India <em>Manuscript received 9 July 2009, revised 10 Marc/1 2010, accepted 19 March 2010</em> The 1-arylthiocarhamides (3), 1, 3-diarylthiocarbamides (6), 1,3-diarylcarbamides (7) and 1-aryl-2,4-dithiobiurets (11) have been synthesized by the microwave induced beating of respective reactants for about 30-60 s in solvent free condition. Reaction yields ar

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43

Mopari, Anuja M., and Gajanan V. Korpe. "Synthesis and Structural Studies of N-Maltosylated Aryl Thiobiurets." Asian Journal of Chemistry 34, no. 5 (2022): 1220–24. http://dx.doi.org/10.14233/ajchem.2022.23649.

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The derivatives of urea, thiourea and thiosemicarbazide play an important role in medicinal chemistry by influencing various pharmacological activities. The design and development of novel N-maltosides have emerged as an important class of organic compounds. A series of 1-hepta-O-benzoyl-β-D-Maltosyl- 5-aryl-2-4-thiobiurets are described in present work. By mixing hepta-O-benzoyl→D-maltosyl isocyanates with various aryl thiocarbamides, 1-hepta-O-benzoyl-β-D-maltosyl-5-aryl-2-4-thiobiurets have been synthesized. The identities of this newly synthesized 1-hepta-O-benzoyl-β-D-Maltosyl-5- aryl-2-4

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44

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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45

Pradip, P. Deohate, P. Deohatc Jyoti, and N. Berad B. "Synthesis of novel benzo-1,2,5-thiadiazines, their antimicrobial activity and isomerization into benzo-1,2,4-triazines." Journal of India Chemical Society Vol 81, Sep 2004 (2004): 775–77. https://doi.org/10.5281/zenodo.5833095.

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P. G. Department of Chemistry, Shri Shivaji Science College, Amravati-444 603, India <em>E-mail</em>: pradip222091 @yahoo.co.in <em>Manuscript received 23 April 2003. revised 12 March 2004. accepted 6 April 2004</em> Benzo[<em>c</em>]-6-aryl/alkylimino-1,2,5-thiadiazines (4a-g) have been obtained by the basification of benzo[<em>c</em>]-6-aryl/alkylimino-1 ,2,5- thiadiazine dihydroiodides (3a-g). The latter were synthesized by the oxidative cyclisation of substituted 1-aryl/alkyl- 3-(2' -aminophenyl)thiocarbamides (2a-g) by ethanolic iodine. Compounds (4a-g) on acylation with acetic anhydr

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46

Ajibola, Risikat O., and Reuben H. Simoyi. "S-Oxygenation of Thiocarbamides IV: Kinetics of Oxidation of Tetramethylthiourea by Aqueous Bromine and Acidic Bromate." Journal of Physical Chemistry A 115, no. 13 (2011): 2735–44. http://dx.doi.org/10.1021/jp1124052.

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47

Mizrakh, L. I., L. Yu Polonskaya, A. N. Gvozdetskii, A. M. Vasil'ev, T. M. Ivanova, and N. I. Lisina. "Synthesis and study of the antiradiation properties of some derivatives of N-allyl-N?-substituted thiocarbamides." Pharmaceutical Chemistry Journal 21, no. 3 (1987): 210–17. http://dx.doi.org/10.1007/bf01146186.

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48

Desai, Ranchhodji Dajibhai, Robert Fergus Hunter та Lakshman Gopal Koppar. "The condensation of thiocarbamides with monochloroacetic acid and the conversion of Arylformamidinethiolacetic acids into ψ-thiohydantoin derivatives". Recueil des Travaux Chimiques des Pays-Bas 54, № 2 (2010): 118–21. http://dx.doi.org/10.1002/recl.19350540208.

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49

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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50

Potikha, L. M., A. V. Turov та V. A. Kovtunenko. "Condensation of γ-bromodypnone with thiocarbamides: Synthesis of 4,4-disubstituted 4,5-dihydro-1,3-thiazol-2-amines and thiazolidin-2-ones". Chemistry of Heterocyclic Compounds 44, № 1 (2008): 86–91. http://dx.doi.org/10.1007/s10593-008-0008-6.

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