Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rajeesh Pakkath"'
Autor:
Ranjith Pakkath Karuvalam, Karickal Raman Haridas, Ayyiliath Meleveettil Sajith, Rajeesh Pakkath, Savitha Bhaskaran, M. Syed Ali Padusha, Vasiliy A. Bakulev, Muthipeedika Nibin Joy
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 431-445 (2020)
Externí odkaz:
https://doaj.org/article/5b73af25b90346caa02b0b634456fb04
Autor:
Savitha Bhaskaran, M. Syed Ali Padusha, Ayyiliath M. Sajith, Vasiliy A. Bakulev, Muthipeedika Nibin Joy, Rajeesh Pakkath, Ranjith P. Karuvalam, Karickal R. Haridas
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 431-445 (2020)
Arkivoc
Arkivoc
An expedient, palladium-mediated cross-coupling approach to functionalize the benzimidazole-based core under microwave-assisted conditions has been developed and is described. This protocol, which incorporates appendage diversity on this potential sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbecb3a4ba302f45a72e2fa11e030c90
https://doi.org/10.24820/ark.5550190.p011.121
https://doi.org/10.24820/ark.5550190.p011.121
Autor:
A. Muralidharan, Koti Reddy Eeda, Rathnasamy Rishikesan, Ranjith P. Karuvalam, Rajeesh Pakkath, Nibin Joy Muthipeedika, Ayyiliath M. Sajith, Karickal R. Haridas, Vaishnav Bhaskar, Kereyagalahally H. Narasimhamurthy
Publikováno v:
Journal of Chemical Sciences. 133
A novel series of analogues based on 5-(1-(4-chloro-3-methoxyphenyl)piperidin-4-yl)-4-phenyl-2H-1,2,4-triazole-3(4H)-thione core have been synthesized and their potential as antibacterial, antifungal and antitubercular agents was examined. The struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9c3c78154dd655ed8b5acb88815e1f2
https://doi.org/10.1007/s12039-020-01872-4
https://doi.org/10.1007/s12039-020-01872-4
Autor:
Eeda Koti Reddy, Bhaskaran Savitha, M. Syed Ali Padusha, Rajeesh Pakkath, C.S. Ananda Kumar, Karickal R. Haridas, D. Parthasarathi, Ayyiliath M. Sajith
Publikováno v:
Journal of Heterocyclic Chemistry. 55:2277-2283
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::414e217d526cc47e3e8966f11ffe42b0
https://doi.org/10.1002/jhet.3280
https://doi.org/10.1002/jhet.3280
Publikováno v:
European Journal of Medicinal Chemistry. 71:354-365
In this paper we report the SAR studies of a series of N-(4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenyl)amide and N-(4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenyl)sulfonamide derivatives 6(a-o) and 7(a-o), were synthesized in good yields and characte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a07f5cd6e832e95f1d56f72031eeb8b
https://doi.org/10.1016/j.ejmech.2013.11.002
https://doi.org/10.1016/j.ejmech.2013.11.002
Autor:
Ranjith P. Karuvalam, Rathnasamy Rishikesan, Nalilu Suchetha Kumari, Karickal R. Haridas, Rajeesh Pakkath
Publikováno v:
Medicinal Chemistry Research. 22:4437-4454
In this article, we report herein the SAR studies of a series of (1H-indol-3-yl)alkyl-3-(1H-indol-3-yl)propanamide 10(a–j), 11(a–j). The synthesized compounds were evaluated for their preliminary in vitro antibacterial, antifungal activity and we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0352b34bcbcff1f92b7e9417370dbbd0
https://doi.org/10.1007/s00044-012-0451-x
https://doi.org/10.1007/s00044-012-0451-x