Zobrazeno 1 - 7
of 7
pro vyhledávání: '"PALUSA SANATH KUMAR GOUD"'
Autor:
NALILU SUCHETHA KUMARI, PALUSA SANATH KUMAR GOUD, RAMASWAMY VENKAT RAGAVAN, KASI REGURAMAN JAI SANKAR, KUBARAN KUMARAN, SUBAN SHAFI SYED, VARADARAJI DHAYANITHI, HARI NARAYAN PATI
Publikováno v:
Journal of the Serbian Chemical Society, Vol 76, Iss 2, Pp 165-175 (2011)
Several 5-thio-substituted tetrazole derivatives were efficiently synthesized by a three-step process. The substituted tetrazol-5-thiol, namely, 1-benzyl-1H-tetrazole-5-thiol (2) was prepared by refluxing commercially available benzyl isothiocyanate
Externí odkaz:
https://doaj.org/article/a3b23a956de149128bbd305d26417dac
Akademický článek
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Publikováno v:
New Journal of Chemistry; 6/7/2024, Vol. 48 Issue 21, p9589-9610, 22p
Autor:
Palusa, Sanath Kumar Goud1,2, Udupi, Rajgopal H.2 udupirh@rediffmail.com, V., Himabindu1, Sridhara, Ajjanna M.3
Publikováno v:
Organic Communications. 2011, Vol. 4 Issue 4, p82-93. 12p.
Akademický článek
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Autor:
Palusa Sanath Kumar Goud, S. K. Peethambar, A. M. Sridhara, Bankavadi C. Somashekar, P.S.C. Bose, Satish Kumar Gaddam, Jathi Keshavayya, Kallam R. Venugopala Reddy
Publikováno v:
European Journal of Medicinal Chemistry. 45:4983-4989
A series of new 2-substituted [4-(1,3,4-oxadiazol-2-yl)methyl]phthalazin-1(2H)-one derivatives 7a-h to 9a-h were designed and synthesized from methyl (4-oxo-3,4-dihydrophthalazin-1-yl)acetate (4), which in was turn prepared from phthalic anhydride. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ea4115bad029e4d2c02461705982597
https://doi.org/10.1016/j.ejmech.2010.08.005
https://doi.org/10.1016/j.ejmech.2010.08.005
Autor:
Manjunath Moger, Rahul Shivahare, Vadiraj S. Gopinath, Mukkavilli Subba Rao, Palusa Sanath Kumar Goud, Denis Martin, P.S.C. Bose, Preeti Vishwakarma, Jakir Pinjari, Vikram Ramanathan, Aditya Verma, Delphine Launay, Sunil K. Puri, Ravindra T. Dere, Suman Gupta
Publikováno v:
European journal of medicinal chemistry. 69
An analogous library of 2-substituted quinoline compounds was synthesized with the aim to identify a potential drug candidate to treat visceral leishmaniasis. These molecules were tested for their in vitro and in vivo biological activity against Leis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c06554ea41ec57306a0dd1bc6b0b35e4
https://pubmed.ncbi.nlm.nih.gov/24095747
https://pubmed.ncbi.nlm.nih.gov/24095747