Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Rangappa Santosh"'
Autor:
Vinuta Kamat, Rangappa Santosh, Boja Poojary, Suresh P. Nayak, Banoth Karan Kumar, Murugesan Sankaranarayanan, Faheem, Sheela Khanapure, Delicia Avilla. Barretto, Shyam K. Vootla
Publikováno v:
ACS Omega, Vol 5, Iss 39, Pp 25228-25239 (2020)
Externí odkaz:
https://doaj.org/article/bcdbba759aa5402e91bb01af2f09eea4
Publikováno v:
Molbank, Vol 2019, Iss 2, p M1058 (2019)
5-methyl-2-(pyridin-3-yl)-1,3-thiazole-4-carbohydrazide (1) on treatment with 4-fluorobenzaldehyde in presence of catalytic amount of acetic acid, accessed the target compound (2) with the yield of 79%. The target compound was confirmed by 1H-NMR, 13
Externí odkaz:
https://doaj.org/article/07cafb8f9cd74ca39ea7d820df9c466d
Autor:
Rangappa Santosh, Ashwini Prabhu, Mukunthan K. Selvam, Panchangam M. Krishna, Gundibasappa K. Nagaraja, Punchappady D. Rekha
Publikováno v:
Heliyon, Vol 5, Iss 2, Pp e01255- (2019)
A series of oxadiazole (7a-l) and hydroxypyrazoline derivatives (8a-l) incorporating thiazole were synthesized and characterized by spectral analysis (1H-NMR, 13C-NMR, Mass, and FT-IR). The synthesized compounds were screened for their in vitro cytot
Externí odkaz:
https://doaj.org/article/5631b6aac5fd4ef7aeb6404b137c8e2b
Autor:
Banoth Karan Kumar, Boja Poojary, Suresh P. Nayak, Sheela Khanapure, Vinuta Kamat, Shyam Kumar Vootla, Delicia A. Barretto, Rangappa Santosh, Faheem, Murugesan Sankaranarayanan
Publikováno v:
ACS Omega, Vol 5, Iss 39, Pp 25228-25239 (2020)
A new class of compounds formed by the linkage of -C(O)-NH- with pyridine and thiazole moieties was designed, synthesized, and characterized by various spectral approaches. The newly characterized compounds were evaluated for their antimicrobial as w
Autor:
Jamballi G. Manjunatha, Priyodip Paul, Mukunthan K. Selvam, Panchangam Murali Krishna, Gundibasappa Karikannar Nagaraja, Rangappa Santosh, Chenthattil Raril
Publikováno v:
ChemistrySelect. 4:990-996
Dihydropyrimidinones (DHPMs), 4a-f and 6a-f is reported and were characterized by 1H-NMR, 13C-NMR, FT-IR and LC–MS. The synthesized compounds were evaluated for their antibacterial activity against Staphylococcus aureus (S.aureus), Bacillus subtili
Publikováno v:
ChemistrySelect. 3:6338-6343
In the current study, an efficient synthesis of new triazole-linked chalcone 3a-g scaffold was performed by multistep reaction sequence and was screened for their antibacterial activity against Pseudomonas aeruginosa, Escherchia coli, Staphylococcus
Autor:
Madan S. Kumar, Gundibasappa Karikannar Nagaraja, Rangappa Santosh, Mukunthan K. Selvam, Saptami Kanekar
Publikováno v:
ChemistrySelect. 3:3892-3898
A series of thiazoles 4a-g and thiazole clubbed triazoles 5a-f were synthesized and showed good antibacterial activity against, Pseudomonas aeruginosa, Escherchia coli, Staphylococcus aureus and Bacillus subtilis. Particularly, 4a (methyl), 5b (nitro
Publikováno v:
Molbank, Vol 2019, Iss 2, p M1058 (2019)
5-methyl-2-(pyridin-3-yl)-1,3-thiazole-4-carbohydrazide (1) on treatment with 4-fluorobenzaldehyde in presence of catalytic amount of acetic acid, accessed the target compound (2) with the yield of 79%. The target compound was confirmed by 1H-NMR, 13
Autor:
Ashwini Prabhu, Punchappady D. Rekha, Rangappa Santosh, Mukunthan K. Selvam, Panchangam Murali Krishna, Gundibasappa Karikannar Nagaraja
Publikováno v:
Heliyon
Heliyon, Vol 5, Iss 2, Pp e01255-(2019)
Heliyon, Vol 5, Iss 2, Pp e01255-(2019)
A series of oxadiazole (7a-l) and hydroxypyrazoline derivatives (8a-l) incorporating thiazole were synthesized and characterized by spectral analysis (1H-NMR, 13C-NMR, Mass, and FT-IR). The synthesized compounds were screened for their in vitro cytot