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Journal articles on the topic 'Benzyl thiocarbamide'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

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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2

D., C. Dash, K. Panda A., Mahapatra A., and B. Patjoshi S. "Synthesis of complexes of N-benzoyl-N' -(2-hydroxyphenyl)thiocarbaniide with some bivalent transition metal ions." Journal of Indian Chemical Society Vol. 79, Aug 2002 (2002): 642–44. https://doi.org/10.5281/zenodo.5843241.

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P. G. Department of Chemistry, Sambalpur University, Jyoti Vihar, Burla, Sambalpur-768 019. India <em>E-mail : </em>dcdash@rediffmail.com <em>Manuscript received 21 May 2001, revised </em>9 <em>November 2001, accepted 21 March 2002</em> A series of binuclear complexes of types [M<sub>2</sub>(BPT)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>] and [M<sub>2</sub>(BPT)<sub>2</sub>L<sub>4</sub>], where H<sub>2</sub>BPT = <em>N</em>-benzoyl-<em>N'</em>-(2-hydroxyphenyl)- thiocarbamide, L = pyridine or picolines (a,(3,7), M = Cu<sup>ll</sup>, Co<sup>ll</sup> and Ni<sup>ll</sup> have been synthesized.

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3

Tewari, Amit, and Rajendra S. Bhakuni. "Thiocarbamates from Moringa Oleifera." Natural Product Communications 1, no. 9 (2006): 1934578X0600100. http://dx.doi.org/10.1177/1934578x0600100905.

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Two new thiocarbamates (1 and 2) along with two known compounds have been isolated from the ethyl acetate extract of Moringa oleifera seeds. The new compounds were characterized as O-n-butyl-4-[(α-L-rhamnopyranosyloxy)benzyl] thiocarbamate (E) (1) and O-ethyl-4–[(α-L-rhamnopyranosyloxy)–3-hydroxybenzyl]thiocarbamate (E) (2) on the basis of 1D and 2D NMR spectroscopic data and MS analysis.

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4

Montiel-Ortega, Luis Alberto, Susana Rojas-Lima, Elena Otazo-Sanchez, and Roberto Villagómez-Ibarra. "O-benzyl-N-(2-furoyl)thiocarbamate." Journal of Chemical Crystallography 34, no. 2 (2004): 89–93. http://dx.doi.org/10.1023/b:jocc.0000014694.33182.ff.

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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

K., C. SATAPAmY, C. DASH D., C. PRADHAN G., and NAIK A. "Cobalt(II), Nickel(II) and Copper(II) Complexes with N-Benzoyl- N ' -(1,3,4-thiadiazol-2- yl)thiocarbamide as Ligand." Journal of Indian Chemical Society Vol. 66, May 1988 (1989): 291–92. https://doi.org/10.5281/zenodo.5948709.

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Department of Chemistry, Sambalpur University, Jyoti Vihar, Burla-768 017 <em>Manuscript received 29 December 1987, revised 26 July 1988, accepted 22 February 1989</em> Complexes of <em>N</em>-benzoyl-N'-(1,3,4-thiadlazol-2-yl)thiocarbamide (L) of composition [ML<sub>2</sub>X<sub>2</sub>) where M -(o<sup>II</sup>, Ni<sup>ll</sup>, Cu<sup>ll</sup>; X-CI. Br, NO<sub>3</sub>, and CIO<sub>4</sub>, have been syn- thesised and characterised on the basis of elemental analysis, conductivity, magnetic and spectral data. The coordination of thiocarbonyl sulphur, carbonyl oxygen of thiocarbamide and

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7

Purkait, Rakesh, Suvendu Maity, and Chittaranjan Sinha. "A hydrazine-based thiocarbamide probe for colorimetric and turn-on fluorometric detection of PO43− and AsO33− in semi-aqueous medium." New Journal of Chemistry 42, no. 8 (2018): 6236–46. http://dx.doi.org/10.1039/c7nj04533f.

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20% of the population in West Bengal, India is at risk to fatal levels of arsenic. Easy detection of As(iii) is demonstrated by the naked eye using a hydrazine-based thiocarbamide reagent. Limit of detection is 15 nM (AsO<sub>3</sub><sup>3−</sup>) at pH 8–12.

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8

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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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

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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11

Zhang, Qiang, Yves Queneau, and Laurent Soulère. "Biological Evaluation and Docking Studies of New Carbamate, Thiocarbamate, and Hydrazide Analogues of Acyl Homoserine Lactones as Vibrio fischeri-Quorum Sensing Modulators." Biomolecules 10, no. 3 (2020): 455. http://dx.doi.org/10.3390/biom10030455.

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A series of carbamate, thiocarbamate, and hydrazide analogues of acylhomoserine lactones (AHLs) were synthesized and their ability to modulate Vibrio fischeri-quorum sensing was evaluated. The compounds in the series exhibit variable side chain length and the possible presence of a diversely substituted phenyl substituent. Biological evaluation on the Vibrio fischeri quorum sensing system revealed that the ethyl substituted carbamate (1) display a weak agonistic activity whereas compounds with longer chain length or benzyl substituents display significant antagonistic activity. The most active

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12

Channar, Pervaiz Ali, Aamer Saeed, Fayaz Ali Larik, et al. "An intramolecular 1,5-chalcogen bond on the conformational preference of carbonyl thiocarbamate species." New Journal of Chemistry 44, no. 14 (2020): 5243–53. http://dx.doi.org/10.1039/c9nj06417f.

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Two closely related carbamothioates were prepared by the reaction of benzoyl isothiocyanates and methanol. The crystal structures show the occurrence of 1,5-O⋯O intramolecular short distance that determines the conformational preference.

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13

Zhang, Shu-Sheng, Jie-Hua Lin, Fang-Fang Jian та Kui Jiao. "Structures of N- (2,3,4,6-Tetra-O-acetyl-β-D-glycosyl) thiocarbamic Benzoyl Hydrazine". Chinese Journal of Chemistry 20, № 2 (2010): 183–86. http://dx.doi.org/10.1002/cjoc.20020200213.

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14

Heda, Kavita. M. "Newly synthesized compounds from 2- hydrazino benzothiazole: Characterization, and evaluation of their antibacterial potential." International Journal of Advance and Applied Research 5, no. 23 (2024): 291–94. https://doi.org/10.5281/zenodo.13622529.

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Abstract:Serial of 1-tetra-O-benzoyl-β-D-glucosyl-3-(2)-hydrazino-1, 3-substituted benzothiozolyl thiocarbamide has been synthesized by the interaction  of   two pharmocophores,  tetra-O-benzoyl-β-D-glucosyl isothiocyanates and amine substituted 2-hydrazino-1,3-benzothiazoles in acetone medium. The reaction mixture was kept at room temp for 24 hrs. In acetone medium. Acetone is evaporated then product is recrystallised by petroleum ether (60-80%).  Benz-fused compounds have been employed in the synthesis of various compounds which show very potential pharmacologic

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15

Gray, Reed A., and Grant K. Joo. "Reduction in Weed Control After Repeat Applications of Thiocarbamate and Other Herbicides." Weed Science 33, no. 5 (1985): 698–702. http://dx.doi.org/10.1017/s0043174500083119.

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Of 17 thiocarbamate herbicides tested in the greenhouse in repeat soil applications made 4 to 16 weeks apart, 9 showed definite losses in herbicidal activity after the second application. Those showing reduced activity included EPTC (S-ethyl dipropylthiocarbamate), vernolate (S-propyl dipropylthiocarbamate), and butylate (S-ethyl diisobutylthiocarbamate), which have been reported previously to develop accelerated breakdown, plus R-15574 (S-benzyl dipropylthiocarbamate and the sulfoxides of EPTC, vernolate, butylate, SC-7829 (S-propyl diisobutylthiocarbamate), and SC-8149 (S-butyl diisobutylthi

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16

Pradip, P. Deohate. "Substituted [1,3,4]-oxadiazole, [1,3,4]-thiadiazole and [1,2,4]-triazole; synthesis, characterization and antimicrobial study." Journal of Indian Chemical Society Vol. 89, Feb 2012 (2012): 253–59. https://doi.org/10.5281/zenodo.5759585.

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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 06 August 2009, revised 29 December 2010, accepted 20 June 2011</em> Series of compounds 5-(benzotriazol-1-yl-methyl)-2-aryl/alkyl-amino-[1 ,3,4]-oxadiazoles, 5-(benzotriazol-1-yl-methyl)-2-ary 1/ alky 1-amino-[1 ,3, 4]-thiadiazoles and 5-(benzotriazol-1-yl-methyl)-3-merca pto-4-aryl/ alkyl-4<em>H</em>-[1 ,2 ,4]-triazoles have been synthesized by the oxidative cyclization of 2-benzotriazol-1-yl-<em>N</em>-aryl/a

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17

Pradip, P. Deohate, and N. Berad B. "Synthesis, characterization and antimicrobial study of substituted bis-[1 ,3,4]-oxadiazole, bis-[1 ,3,4]-thiadiazole and bis-[1,2,4]-triazole derivatives." Journal of Indian Chemical Society Vol. 85, Nov 2008 (2008): 1153–58. https://doi.org/10.5281/zenodo.5820567.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : pradip22209l@yahoo.co.in Postgraduate Department of Chemistry, Shri Shivaji Science College, Amravati-444 603, Maharashtra, India <em>Manuscript received 29 April 2008, accepted 16 July 2008</em> Series of compounds 1,4-bis-(2-aryl/alky1-amino-[1,3,4]-oxadiazol-5-yI)-benzenes, 1,4-bis-(2-aryl/alkyl-amino[ 1,3,4]-thiadiazol-5-yl)-benzenes and 1,4-bis-(3-mercapto-4-aryl/alkyl-[1,2,4]-triazol-5-yl)-benzenes have been synthesized by the oxidative cyclization of di

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18

Arkhipova, A. V., K. V. Malkova, T. N. Sokolova, and V. R. Kartashov. "Synthesis of a new thiocarbamate by the reaction of benzyl thiocyanate with camphene, catalyzed by heteropoly acids." Russian Journal of Applied Chemistry 80, no. 1 (2007): 162–63. http://dx.doi.org/10.1134/s1070427207010338.

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19

Kutyreva, M. P., A. F. Maksimov, A. M. P. Ernandes, A. A. Zhukova, A. R. Gataulina, and G. A. Kutyrev. "Interaction of Poly(benzoyl thiocarbamate)-Modified Hyperbranched Polyester with Co(II) and Cu(II) Nitrates." Russian Journal of General Chemistry 90, no. 2 (2020): 268–73. http://dx.doi.org/10.1134/s1070363220020164.

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20

Dong, Zhonglin, Tao Jiang, Bin Xu, Qian Li, Hong Zhong, and Yongbin Yang. "Selective flotation of galena using a novel collector S-benzyl-N-ethoxycarbonyl thiocarbamate: An experimental and theoretical investigation." Journal of Molecular Liquids 330 (May 2021): 115643. http://dx.doi.org/10.1016/j.molliq.2021.115643.

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21

Guo, Junxiang, Yaqin Chai, Ruo Yuan, Yuhua Ma, and Zhifen Zou. "A Fast Response Strontium(II) Selective Polymeric Membrane Sensor Based on 1–Benzothiazol–3–Benzoyl–Thiocarbamide as Neutral Carrier." Sensor Letters 8, no. 4 (2010): 596–601. http://dx.doi.org/10.1166/sl.2010.1317.

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22

Hamdy, Rania, Arwyn T. Jones, Mohamed El-Sadek, et al. "New Bioactive Fused Triazolothiadiazoles as Bcl-2-Targeted Anticancer Agents." International Journal of Molecular Sciences 22, no. 22 (2021): 12272. http://dx.doi.org/10.3390/ijms222212272.

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A series of 3-(6-substituted phenyl-[1,2,4]-triazolo[3,4-b]-[1,3,4]-thiadiazol-3-yl)-1H-indoles (5a–l) were designed, synthesized and evaluated for anti-apoptotic Bcl-2-inhibitory activity. Synthesis of the target compounds was readily accomplished through a reaction of acyl hydrazide (1) with carbon disulfide in the presence of alcoholic potassium hydroxide to afford the corresponding intermediate potassium thiocarbamate salt (2), which underwent cyclization reaction in the presence of excess hydrazine hydrate to the corresponding triazole thiol (3). Further cyclisation reaction with substitu

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23

Rybakov, V. B., L. G. Boboshko, N. I. Burakov, et al. "X-ray mapping in heterocyclic design: XI. X-ray diffraction study of 1-benzoyl-3-(pyridin-2-yl)-thiocarbamide and the product of its reaction with oxidants." Crystallography Reports 48, no. 4 (2003): 576–82. http://dx.doi.org/10.1134/1.1595182.

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24

Swapnil, V. Nakat, and M. Thorat Sharayu. "REDUCTIVE DESULFURIZATION OF N- SUBSTITUTED THIOCARBAMIDES TO FORMAMIDINES VIA RANEY-NICKEL." October 30, 2022. https://doi.org/10.5281/zenodo.7264371.

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<em>A novel synthesis of </em><em>N</em><em>-benzyl-N’-[2-(N’-benzyl-formimidoylamino)- N-substituted]-formamidine has been synthesized by reductive desulfurization of 1-benzyl-3-[2-(3-benzyl-thioureido)-substituted]-thiocarbamide by Raney-Nickel in toluene medium. The identities of these new N-substituted formamidine derivative have been established on the basis of usual chemical transformation and IR, NMR, and 13C spectra.</em>  

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25

Apaydın, Çağla Begüm, Özge Soylu-Eter, Pınar Eraslan-Elma, Nurten Özsoy, and Nilgün Karalı. "Synthesis and molecular modeling studies of 1-benzyl-2-indolinones as selective AChE inhibitors." Future Medicinal Chemistry, December 16, 2022. http://dx.doi.org/10.4155/fmc-2022-0139.

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Background: Possible bioisosteres can be developed by replacing the 1-indanone ring (one of three pharmacophore groups) of donepezil with an indoline ring. As H2S donors, thioamide, thiocarbamate and thiourea groups are also critically important. Materials & methods: The 1-benzyl-2-indolinones 6a–n were designed using molecular modeling and synthesized, and their acetylcholinesterase and butyrylcholinesterase inhibitory effects were then investigated. Results: The compounds 6h (inhibition constant [ Ki] = 0.22 μM; selectivity index [SI] = 26.22), 6i ( Ki = 0.24 μM; SI = 25.83), 6k ( Ki = 0

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26

Duc, Ha Danh. "Anaerobic degradation of thiobencarb by mixed culture of isolated bacteria." FEMS Microbiology Letters, December 15, 2022. http://dx.doi.org/10.1093/femsle/fnac123.

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Abstract Thiobencarb is a highly effective thiocarbamate herbicide frequently used in rice fields globally. In this study, three bacterial strains (Dechloromonas sp. Th1, Thauera sp. Th2, and Azoarcus sp. Th3) isolated from immobilized biomass were analyzed for thiobencarb degradation under anaerobic conditions, with nitrate serving as an electron acceptor. The experimental results showed that thiobencarb was transformed by Dechloromonas sp. Th1 and Thauera sp. Th2 to produce high concentrations of metabolites in a mineral medium. Dechloromonas sp. Th1 dechlorinated the herbicide to benzyl mer

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