Relevant bibliographies by topics / Benzyl thiocarbamide

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Academic literature on the topic 'Benzyl thiocarbamide'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Benzyl thiocarbamide"

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&#39;</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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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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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-&beta;-D-maltosyl-3-aryl thiocarbamides, 1-hepta-<em>O</em>-benzoyl-&beta;-D-maltosyl-3-substituted benzothiazolyl thiocarbamides and 1-hepta-<em>O</em>-benzoyl-&beta;-D-maltosyl-0-alkyl thiocarbamates on reac
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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&#39;-(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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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-&beta;-D-lactosylimino-3-hepta-<em>O</em>-benzoyl-&beta;-D-lactosylimino-1,2,4-dithiazolidines (hydrochloride) have been synthesized by the interaction of various 1-hepta-<em>O</em>-benzoyl-&beta;-D-lactosyl-3-aryl thiocarbamides with <em>N</em>-hepta-<em>O</em>
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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-&beta;-D-lactosyl-3-aryl thiocarbamides and <em>N</em>-phenyl-<em>S</em>-chloro isothiocarbamoyl chloride a
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Book chapters on the topic "Benzyl thiocarbamide"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of binuclear nickel(II) complex with N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_282.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of binuclear copper(II) complex with N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_564.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamido]tetrapyridinedicobalt(II,II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_435.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of tetraaqua-bis[N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamido]dicobalt(II,II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_434.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand binuclear nickel(II) complex with N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamide and pyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_283.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand binuclear copper(II) complex with N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamide and pyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_565.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamido]tetra(α-picoline)dicobalt(II,II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_438.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamido]tetra(β-picoline)dicobalt(II,II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_436.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamido]tetra(ϒ-picoline)dicobalt(II,II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_437.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand binuclear nickel(II) complex with N-benzoyl-N′-(2-hydroxyphenyl)-thiocarbamide and α-picoline." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_284.

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