Zobrazeno 1 - 10 of 45 pro vyhledávání: '"M. G. Paranjpe"'
2
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
Autor: (MRS)V. J. APARAJIT, M. G. PARANJPE
Department of Chemistry, Nagpur University Campus, Amravati Road, Nagpur-440 010 Manuscript received 26 September 1991, revised 6 January 1993, accepted 29 March 1993 SeveraI 2-mercapto-t-butyl-3-t-butyl-4-phenylim ino-5-a ryl/alkyl-6-thio-tetrahydro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ab1f62e3e714f3531b1e7f49ec65e7e
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3
On Glucosyl Thioureides. Part-IV. Synthesis of 3-Aryl-2,6-diphenylimino-4-5 tetra-O-acetyl-D-glucopyranosyl-5,6-dihydro-1,3,5-thiacliazine (Hysrochlorides)
Autor: (Miss) I. D. BllDEKAR, M. G. PARANJPE
Department of Chemistry, Nagpur University, Nagpur-440 010 Manuscript received 12 July 1982, revised 10 April 1984, accepted 75 August 1984 Certain 3-aryl-2,6-diphenylimino-4-S-tetra-O-acetyl-D-glucopyranosyl-5,6- dihydro­l,3,5-thiadiazines (hydroch
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14cf0717bde6c039806d6d1bd1054bec
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9
3-Oxo-5-Phenylimino-1 ,2,4-thiadiazolidine and lts Some Aryl Analogues
Autor: N. M. NIMDEOKAR, M. G. PARANJPE
University Chemistry Department, Nagpur-440 010 Manuscript received 27 February 1980, accepted 7 August 1980 Certain 3-oxo-2 - unsubstituted/aryl substituted-4-unsubstituted/aryl substituted-5- phenylimino-1,2,4-thiadiazolidines involving interaction
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f7150104747071893a5dcaa8c48d48
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10
ChemInform Abstract: S-CHLORO-N-PHENYL THIOCARBAMOYL CHLORIDE AS AN INTERMEDIATE IN HETEROCYCLIC SYNTHESIS
Autor: M. G. Paranjpe, A. S. Mahajan, V. S. Kamble
Publikováno v: Chemischer Informationsdienst. 6
Durch Kondensation von Phenylthiocarbamid (Ia) bzw. p-Chlorphenylthiocarbamid (Ib) mit S-Chloro-N-phenyl-thiocarbamoylchlorid (II) in wasserfreiem Benzol bei 80°C entstehen die Hexahydrotriazinderivate (III), deren Umsetzung mit Benzylchlorid zu den
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::80bae86dc8228cd6cc0637c89ac6aec6
https://doi.org/10.1002/chin.197509296
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