Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Pramod P. Kattimani"'
Novel pyrazole derivativesviaring transformations: Anti-inflammatory and antifungal activity studies
Autor:
Pramod P. Kattimani, Ravindra R. Kamble, Sunil Jalalpure, Aravind R. Nesaragi, Shrinivas D. Joshi, Suneel Dodamani, Mahadevappa Y. Kariduraganavar
Publikováno v:
Synthetic Communications. 51:3125-3140
In this paper, the synthesis of novel pyrazoles and their in vitro anti-inflammatory and in-vitro antifungal assay have been reported. These compounds were docked into the inducible nitric oxide sy...
Publikováno v:
Arabian Journal of Chemistry, Vol 9, Iss S1, Pp S306-S312 (2016)
A novel one-pot synthesis of sydnones appended to coumarins (4a–r) via thiazole in presence of silica sulfuric acid as a heterogeneous catalyst is discussed. The use of low cost and reusable silica sulfuric acid as catalyst makes this process feasi
Externí odkaz:
https://doaj.org/article/5273f052b4714e6381f235a9b07d618c
Publikováno v:
Microwave Heating-Electromagnetic Fields Causing Thermal and Non-Thermal Effects ISBN: 9781839682261
Microwave chemistry involves the application of microwave radiation to chemical reactions and has played an important role in organic synthesis. Functional dyes are those with hi-tech applications and this chapter attempts to provide an overview of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::692cf05cf1f151d7320911a2df2b5f8f
https://doi.org/10.5772/intechopen.94946
https://doi.org/10.5772/intechopen.94946
Autor:
Pramod P. Kattimani, Ravindra R. Kamble, Mahadev N. Kumbar, H. K. Arunkashi, H. C. Devarajegowda
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 4, Pp o499-o499 (2014)
In the title compound, C8H6ClN3O, the dihedral angle between the 1,2,4-triazole and benzene rings is 4.60 (9)° and an intramolecular C—H...O interaction closes an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H...O hydrogen bo
Externí odkaz:
https://doaj.org/article/05d3508ae7844a94bf79aa6ce8f3a8c3
Autor:
Shrinivas D. Joshi, Ravindra R. Kamble, Pramod P. Kattimani, Shilpa M. Somagond, H. C. Devarajegowda, Saba Kauser J. Shaikh, Sheshagiri R. Dixit
Publikováno v:
ChemistrySelect. 3:2004-2016
A new series quinoline-2H-1,2,4-triazol-3(4H)-ones 7 g-n and 11 g-n were designed and synthesized. Docking studies of title compounds with DNA (PDB: 1AU5) and with long-chain enoyl-acyl carrier protein reductase (InhA) enzyme (PDB ID: 4TZK) as antica
Autor:
Sheshagiri R. Dixit, Shilpa M. Somagond, Pramod P. Kattimani, Shrinivas D. Joshi, Ravindra R. Kamble
Publikováno v:
Heterocyclic Communications. 23:317-324
Substituted quinolines containing a 1,2,4-triazole moiety were synthesized using reported methods. The molecular docking studies support the experimental results that these compounds are active against A. fumigatus and C. albicans where N-myristoyl t
Autor:
Ravindra R. Kamble, Raveendra K. Hunnur, Shrinivas D. Joshi, Subhas C. Bijjaragi, Shilpa M. Somagond, Praveen K. Bayannavar, Pramod P. Kattimani
Publikováno v:
Drug development researchREFERENCES. 81(1)
In this study, we report the ring transformation of 3-arylsydnone into 1-aryl-1H-pyrazole-3-carbonitriles via [3 + 2] cycloaddition with acrylonitrile. 1-Aryl-1H-pyrazole-3-carbonitrile underwent [2 + 3] cycloaddition with sodium azide to afford 5-(1
Publikováno v:
RSC Advances. 5:29447-29455
In the present report an efficient, rapid, facile and inexpensive route for the synthesis of benzimidazoles using 1,2-arylenediamines and N,N-dimethylformamide in acidic medium under thermal/microwave condition is developed. This reaction was further
Autor:
Atukuri Dorababu, Atulkumar A. Kamble, Ravindra R. Kamble, Mahadevappa Y. Kariduraganavar, Pramod P. Kattimani
Publikováno v:
Letters in Organic Chemistry. 11:244-249
Autor:
Maraswamy Manikantha, Atukuri Dorababu, Joy H. Hoskeri, Pramod P. Kattimani, Tegginamath Gireesh, Ravindra R. Kamble
Publikováno v:
Archiv der Pharmazie. 346:645-653
A novel series of Biginelli 2-3 (a and b) and Biginelli-like compounds 4-7 (a and b) were synthesized from 3-aryl-4-formylsydnone 1 (a and b). Since the crystal structure of hyaluronidase was unavailable, the human hyaluronidase protein structure was