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Journal articles on the topic 'Isodithiobiurets'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

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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2

Prashant, R. Mahalle, and P. Deshmukh Shirish. "Synthesis of N-galactosylated isodithiobiurets." Journal of Indian Chemical Society Vol. 85, July 2008 (2008): 742–45. https://doi.org/10.5281/zenodo.5817164.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India E-mail : prmahalle@rediffmail.com Manuscript received 1 November 2007, accepted 28 April 2008 Several 1-aryl-5-tetra-O-acetyl-β-D-galactosyi-2-S-benzyl-2,4-isodithiobiurets have been prepared by the interaction of aryi-S-benzyl isotbiocarbamides and tetra-O-acetyl-β-D-galactosyl isothiocyanate. The structures of the newly synthesized compounds have been established on the basis of usual chemical transformations and IR, NMR and Mass spectral studies.

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3

R., T. JADHAV, and G. PARANJPE M. "Debenzylation and Oxidative Cyclisation of Certain 2-S-Benzyl-1,5-diaryl-2,4-isodithiobiurets with Elemental Sulphur." Journal of Indian Chemical Society Vol. 62, Feb 1985 (1985): 161–63. https://doi.org/10.5281/zenodo.6321573.

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Depratment of Chemistry, Nagpur University, Nagpur-440 010 <em>Manuscript received 26 July 1982, revised 29 August 1984, accepted 15 February 1985</em> Debenzylation and Oxidative Cyclisation of Certain 2-<em>S</em>-Benzyl-1,5-diaryl-2,4-isodithiobiurets with Elemental Sulphur

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4

Mahalle, Prashant R., and Shirish P. Deshmukh. "Synthesis and Antimicrobial Studies of Some Bis-Glycosyl Isodithiobiurets." E-Journal of Chemistry 7, no. 3 (2010): 795–98. http://dx.doi.org/10.1155/2010/798145.

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Certain 2-S-tetra-O-benzoyl-D-glucopyranosyl-1-aryl-5-tetra-O-acetyl–β-D-galactopyranosyl-2, 4- isodithiobiurets have been synthesized by the interaction of tetra-O-acetyl-β-D-galactopyranosyl isothiocyante and variousS- tetra-O-benzoyl-D- glucopyranosyl-1-aryl isothiocarbamides. The newly synthesized compounds were screened for their antimicrobial activities.

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5

Ghuge, R. D., та S. P. Deshmukh. "ynthesis and Characterization of 1-Aryl-5-hepta-O-acetyl-β-D-maltosyl-2-S-benzyl-2,4-isodithiobiurets". E-Journal of Chemistry 9, № 1 (2012): 330–34. http://dx.doi.org/10.1155/2012/521751.

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The facile synthesis of 1-aryl-5-hepta-o-acetyl-β-D-maltosyl-2-S-benzyl-2,4-isodithiobiurets(IIIa-g)has been achieved by the interaction of 1-hepta-O-acetyl-β–D-maltosyl isothiocyanate(I)with various1-aryl-S-benzyl isothiocarbamides(IIa-g). All the newly synthesizedN-maltosylated compounds characterized by elemental analysis,IR,NMRand Mass spectral studies.

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6

S., K. Bhagat, P. Deshmukh S., and Musaddiq Mohammad. "On glucosyl thioureides : synthesis, antibacterial and antifungal studies of certain 2-S-tetra-0-benzoyl-D-glucopyranosyl-1,5-disubstituted-2,4-isodithiobiurets." Journal of Indian Chemical Society Vol. 80, Oct 2003 (2003): 916–17. https://doi.org/10.5281/zenodo.5839360.

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Department of Chemistry, Department of Microbiology, Shri Shivaji College, Akola-444 001, India <em>Manuscript received 27 August 2001, revised 26 December 2002, accepted 5 May 2003</em> 2-S-Tetra-<em>O</em>-benzoyl-D-glueopyranosyl-1,5-disubstituted-2,4-isodithiobiurets have been prepared by the interaction of S-tetra-<em>O</em>-benzoyl-D-glucopyranosyl aryl isothiocarbamides and <em>p</em>-tolyl isothiocyanate. Antibacterial and antifungal activities of these compounds were evaluated.

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7

G., V. Korpe, та P. Deshmukh S. "Synthesis of 1-tetra-O-benzoyl-β-D-glucopyranosyl-5-aryi-2-S-benzyl2,4-isodithiobiurets and their antimicrobial activity". Journal of Indian Chemical Society Vol. 79, Dec 2002 (2002): 972–73. https://doi.org/10.5281/zenodo.5848491.

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Department of Chemistry. Shri Shivaji College. Akola-444 001 India <em>Manuscript received 17 August 2001.revised 3 April 2002. accepted 16 July 2002</em> 1-Tetra-<em>O</em>-benzoy1-β-D-glucopyranosyl.5-ary1.2-<em>S</em>-benzyl-2,4-isodithiobiurets (4) have been prepared by the interaction of 1-tetra-<em>O</em>-benzoy1-β-D-glucopyranosyl-2<em>S</em>-benzylisothiocarbamide (2) with aryl isothiocyanates (3), and screened for their antibacterial and antifungal activities.

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8

S., K. Bhagat, and P. Deshmukh S. "On glucosylthiourcidcs: synthesis of 3-aryl-2-phenylimino-6-p-tolylimino-4-S-tetra-O-benzoyi-D-glucopyra nosyl-2,3-dihydro-1 ,3,5-thiad iazincs (hydrochlorides) and their antibacterial and antifungal studies." Journal of Indian Chemical Society Vol. 80, Jun 2003 (2003): 654–55. https://doi.org/10.5281/zenodo.5840021.

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Department or Chemistry, Shri Shivaji College, /\kola-444 001, lndia <em>Manuscriet received 3 may 2002. accetcd 2 .January 2003</em> Some 3-aryl-2-phenylimino-6-<em>p</em>-tolylimino-4-tetra-O-betrioyl-n-glucopyranosyl-2,3-dihydro-1,3,5-ihiadiazines (hydrochlorides) have been prepared by the interaction or phenyl isocyanodichloride and 2-S-tetra-<em>O</em>-benzoyl-D-glucopyranosyl-1-aryl-5-p-toly1- 2,4-isodithiobiurets. These compounds show good to moderate antibacterial and antifungal activities. 

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9

Mamta, T. Sangole, and P. Deshmukh Shirish. "Synthesis and characterization of 1-hepta-O-benzoyl-ß-D-maltosyl-5-aryl-2-Sbenzyl- 2,4-isodithiobiurets." Journal of Indian Chemical Society Vol. 88, May 2011 (2011): 743–46. https://doi.org/10.5281/zenodo.5769143.

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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 09 January 2009, revised 08 September 2010, accepted 15 September 2010</em> A series of novel 1-hepta-0-benzoyi-P-o-maltosyl-5-aryi-2-S-benzyl-2,4-isodithiobiurets have been synthesized by the interaction of 1-hepta-β-benzoyl-P-D-maltosyl-S-benzyl isothiocarbamlde with various aryl isothiocyanates. The newly synthesized compounds have been characterized by analytical and IR, <sup>1</sup>H NMR and Mass spectral studies.

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10

S., K. Bhagat, and P. Deshmukh S. "Synthesis of 3-aryl-2-tert.butylimino-6-p-tolylimino-4-(S-tetra-O-benzoyl-D-glucopyranosyl)-2,3-dihydro-1,3,5-thiadiazine hydrochlorides and their antibacterial and antifungal studies." Journal of Indian Chemical Society Vol. 82, Nov 2005 (2005): 1022–24. https://doi.org/10.5281/zenodo.5825057.

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Post-Graduate Department of Chemistry, Shri Shivaji College, Akola-444 001, India <em>Manuscript received 7 July 2005, revised 22 July 2005, accepted 29 July 2005</em> Some 3-aryl-2-tert.butylimino-6-<em>p</em>-tolylimino-4-S-tetra-O-benzoyl-D-glucopyranosyl-2,3-dihydro-1,3,5-thiadiazines (hydrochlorides) have been prepared by the interaction of 2-(S-tetra-<em>O</em>-benzoyl-D-glucopyranosyl)-1-aryl-5-<em>p</em>-tolyl-2,4-isodithiobiurets and tert.butyl isocyanodichloride. These compounds show good to moderate antibacterial and antifungal activities. All products are optically active.

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11

Mamta, T. Sangole, and P. Deshmukh Shirish. "Synthesis of 2-phenylimino-3-aryi-4-S-benzyl-6-hepta-O-benzoyl-ß-Dmaltosylimino- 2,3-dihydro-1 ,3,5-thiadiazines (hydrochloride)." Journal of Indian Chemical Society Vol. 88, May 2011 (2011): 739–42. https://doi.org/10.5281/zenodo.5769133.

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P.O. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India  <em>E-mail</em> : mamtasangole@rediffmail.com <em>Manuscript received 15 December 2008, revised 08 September 2010, accepted 15 September 2010</em> A new series 2-phenylimino-3-aryl-4-S-benzyl-6-hepta-<em>O</em>-benzoyi-β-D-maltosylimino-2,3-dihydro-l,3,5-thiadiazincs (hydrochloride) have been synthesized by the interaction of 1-aryi-S-hepta-O-benzoyl-β-D-maltosyl-2-S-benzyl-2,4-isodithiobiurets with phenyl isocyanodichloride. The newly synthesized compounds have been characterizted by analytic

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12

P., T. Agrawal, та P. Deshmukh S. "Synthesis and antimicrobial activity of 2-phenylimino-3-aryl-4-S-benzyl-6-hepta-0-benzoyl-β-D-lactosylimino-2,3-dihydro-1 ,3,5-thiadiazine hydrochloride". Journal of Indian Chemical Society Vol. 87, Oct 2010 (2010): 1259–62. https://doi.org/10.5281/zenodo.5805038.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashra, India <em>Manuscript received 15 December 2008, revised 26 March 2010, accepted 7 April 2010</em> Several <em>N</em>-lactosylated-1,3,5-thiadiazine hydrochlorides have been prepared by the interaction of 1-aryl-5-hepta-<em>O</em>-benzoyl-β-D-Iactosyl-2-<em>S</em>-benzyl-2,4-isodithiobiurets and phenyl isocyanodichloride. The structure of these new <em>N</em>-lactosylated-1,3,5-thiadiazines have been established on the basis of usual chemical transformations and IR, NMR and Mass spectral analysis. Antimicrobial

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13

P., T. Agrawal, та P. Deshmukh S. "Synthesis and antimicrobial activity of 1-hepta-0-benzoyl-β-D-Iactosyl-5-aryl-2- S-benzyl-2,4-isodithiobiurets". Journal Of India Chemical Society Vol. 87, Nov 2010 (2010): 1395–98. https://doi.org/10.5281/zenodo.5805921.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India Manuscript received 1 January 2009, revised 26 March 2010, accepted 7 April 2010 Several 1-hepta-<em>O</em>-benzoyl-β-D-lactosyl-5-aryl-2-S-benzyl-2,4-isodithiobiurets have been prepared by the interaction of I-hepta-<em>O</em>-benzoyl-β-D-lactosyl-2·S-benzyl isothioearbamide with aryl isothiocyanates. The structure of these new <em>N</em>-lactosylated-2,4-isodlthlobiurets have been established on the basis or usual chemical transformations and IR, NMR, and Mass spectral analysis. Antimicrobi

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14

S., P. DESHMUKH, N. BERAD B., and G. PARANJPE M. "New N-Giucosides. Syntheses of 1- and 5-Glucosyl-2, 4-isodithiobiurets." Journal of Indian Chemical Society Vol. 63, Mar 1986 (1986): 315–16. https://doi.org/10.5281/zenodo.6253755.

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Department of Chemistry, Nagpur University, Nagpur-440 010 <em>Manuscript received 16 December 1984, revised 6 May 1985, accepted 24 December 1985</em> Several   1-tetra-<em>O</em>-acetyl-<em>β</em>-D-glucopyranosyl-5-aryl/alkyl-2-<em>S</em>-benzyl-2-4-isodi-thiobiurets (4) and 1-aryl/(<em>H</em>)-5-tetra-<em>O</em>-acetyl-<em>β</em>-D-glucopyranosyl-2-<em>S</em>-benzyl-2,4-isodithiobiurets (7) have been prepared by the interaction of 1-tetra-<em>O</em>-acetyl-<em>β</em>-D-gincopyranosyl-2-<em>S</em>-benzyl isothiocarbamide with aryljalkylisothiocyanates

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15

Reena, J. Deshmukh, and P. Deshmukh Shirish. "Synthesis and antimicrobial activity of 3-aryl-2,6-diphenylimino-4-S-hepta-O- benzoyl-lactosyl-2,3-dihydro-1 ,3,5-thiadiazine hydrochlorides." Journal of Indian Chemical Society Vol. 90, Jul 2013 (2013): 1027–31. https://doi.org/10.5281/zenodo.5774840.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail </em>: rjdeshmukh22@gmail.com <em>Manuscript received 07 February 2012, revised 04 July 2012, accepted 01 August 2012</em> A new series 3-aryl-2,6-diphenylimino-4-S-hepta-<em>O</em>-benzoyl-lactosyl-2,3-dihydro-1,3,5-thiadiazine hydrochlorides have been synthesized by the interaction of S-hepta-<em>O</em>-benzoyl-lactosyl-1,5-disubstituted-2,4-isodithiobiurets and phenyl isocyanodichloride. The newly synthesized compounds have been characterised by analytical and IR, <sup>1</sup>H NMR and Mass spec

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16

(MRS)V., J. APARAJIT, and G. PARANJPE M. "New s-Triazines : Synthesis of 2-Mercapto-t-butyl-3-tbutyl-4-phenylimino-5-aryl/alkyl-6-thiotetrahydro- and 2-Phenylimino-3-t-butyl-4-phenylimino-5-aryl/alkyl-6-thiohexahydro-1 ,3,5-triazines." Journal of Indian Chemical Society Vol. 70, Oct 1993 (1993): 819–21. https://doi.org/10.5281/zenodo.5929841.

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Department of Chemistry, Nagpur University Campus, Amravati Road, Nagpur-440 010 <em>Manuscript received 26 September 1991, revised 6 January 1993, accepted 29 March 1993</em> SeveraI 2-mercapto-t-butyl-3-t-butyl-4-phenylim ino-5-a ryl/alkyl-6-thio-tetrahydro-1,3,5-triazines have been pepared by the interaction of 1-t-butyl-2-S-t-butyl-5-aryl/alkyl-2,4-isodithiobiurets with phenylisocyanodichloride leading to 2-phenylimino-3-t-butyl-4-mercapto-t-butyl-6-aryl/alkylimino-1,3,5-thiadiazine hydrochlorides followed by isomeric conversion of the latter with aqueous ethanolic sodium bicarbonate/sodiu

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17

D., V. Mangte, and P. Deshmukh S. "Synthesis of 3-aryl-2,6-diphenylimino-4-(S-hepta-O-acetyllactosyl)-2,3-dihydro- 1,3,5-thiadiazine hydrochlorides." Journal of Indian Chemical Society Vol. 83, May 2006 (2006): 517–18. https://doi.org/10.5281/zenodo.5819427.

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Post-Graduate Department of Chemistry. Shri Shivaji College, Akola-444 001, Maharashtra, India E-mail : spd _ dattatraya@rediffmail.com <em>Manuscript received 26 July 2005, revised 14 December 2005, accepted 21 February 2006</em> A scries of 3-aryl-2,6-diphenylimino-4-(S-hepta-\(O\)-acetyl lactosyl)-2,3-dihydro-1,3,5-thiadiazines (hydrochlorides) have been Synthesized by the reaction of S-hepta-\(O\)-acetyl lactosyl-1-aryl-5-phenyl-2,4- sodithiobiurets (I) with phenyl isocyanodichloride (2). The compounds were characterized by IR, NMR and mass spectral analysis.

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18

Sangole, Mamta T., та Shirish P. Deshmukh. "ChemInform Abstract: Synthesis and Characterization of 1-Hepta-O-benzoyl-β-D-maltosyl-5-aryl-2-S-benzyl-2,4-isodithiobiure ts." ChemInform 43, № 11 (2012): no. http://dx.doi.org/10.1002/chin.201211190.

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19

DESHMUKH, S. P., B. N. BERAD, and M. G. PARANJPE. "ChemInform Abstract: New N-Glucosides. Synthesis of 1- and 5-Glucosyl-2,4-isodithiobiurets." ChemInform 18, no. 2 (1987). http://dx.doi.org/10.1002/chin.198702325.

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20

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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21

JADHAV, R. T., and M. G. PARANJPE. "ChemInform Abstract: Debenzylation and Oxidative Cyclisation of Certain 2-S-Benzyl-1,S-diaryl-ZA-isodithiobiurets with Elemental Sulphur." Chemischer Informationsdienst 17, no. 1 (1986). http://dx.doi.org/10.1002/chin.198601193.

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