A novel series of homoallylic amines as potential antimicrobials
| dc.contributor.author | Rai, U.S. | |
| dc.contributor.author | Isloor, A.M. | |
| dc.contributor.author | Shetty, P. | |
| dc.contributor.author | Isloor, N. | |
| dc.contributor.author | Padaki, M. | |
| dc.contributor.author | Fun, H.-K. | |
| dc.date.accessioned | 2026-02-05T09:35:18Z | |
| dc.date.issued | 2012 | |
| dc.description.abstract | An efficient catalytic three-component reaction of aldehydes, amines, and allyltributylstannate has been successfully developed to produce homoallylic amines at 25°C, in excellent yields, in the presence of 1 mol% of trifluoroacetic acid an inexpensive and environmentally friendly catalyst. Newly synthesized compounds were confirmed by spectral studies. Compound 3o was characterized by single crystal X-ray analysis. All the compounds were also screened for their antimicrobial activity. Halogen-substituted compounds namely 3d, 3g, 3n, and 3o have showed excellent antibacterial activity. © Springer Science+Business Media, LLC 2011. | |
| dc.identifier.citation | Medicinal Chemistry Research, 2012, 21, 7, pp. 1090-1097 | |
| dc.identifier.issn | 10542523 | |
| dc.identifier.uri | https://doi.org/10.1007/s00044-011-9607-3 | |
| dc.identifier.uri | https://idr.nitk.ac.in/handle/123456789/26994 | |
| dc.subject | (1 benzofuran 2 yl but 3 eny) napthalen 1 yl amine | |
| dc.subject | (1 benzofuran 2 yl but enyl) (3,5 difluoro benzyl) amine | |
| dc.subject | (1 cyclohexyl but 3 enyl) (2,5 dimethyl phenyl) amine | |
| dc.subject | (1 cyclohexyl but 3 enyl) (4 morpholin 4 yl phenyl) amine | |
| dc.subject | (1 cyclopropyl but 3 enyl) (4 fluoro 3 trifluoromethylphenyl) amine | |
| dc.subject | (2,4 difluoro phenyl) [1(2,4 difluoro phenyl) but 3 enyl] amine | |
| dc.subject | (4 chloro 2 fluoro phenyl) [1(2,6 difluoro phenyl) but 3 enyl] amine | |
| dc.subject | (4 tert butyl phenyl) (1 cyclopropyl 3 but enyl) amine | |
| dc.subject | (4 tert butyl phenyl) [1(2,4 difluoro phenyl) but 3 eny] amine | |
| dc.subject | 1[3(1 (benzothiazol 7 ylamino) but 3 enyl) indol 1 yl] ethanone | |
| dc.subject | 4(1 thiophen 2 yl butylamino) benzonitrile | |
| dc.subject | [1(2 allyloxy phenyl) but 3 enyl][4(4 chloro phenoxy) phenyl] amine | |
| dc.subject | [1(2 fluoro 6 methoxy phenyl) but 3 enyl] (3 fluorophenyl) amine | |
| dc.subject | [1(2,4 diflurophenyl) but 3 enyl] (2,4,5-trifluorophenyl) amine | |
| dc.subject | [1(3 chloro phenyl) but enyl] (3 ethoxy phenyl) amine | |
| dc.subject | [4(4 chloro phenoxy) phenyl] [1(5(2 chloro phenyl) furan 2 yl) but 3 enyl] amine | |
| dc.subject | aldehyde | |
| dc.subject | allyltributylstannate | |
| dc.subject | amine | |
| dc.subject | antiinfective agent | |
| dc.subject | ceftriaxone | |
| dc.subject | halogen | |
| dc.subject | homoallylic amine | |
| dc.subject | naphthalene1 y (1 phenyl but 3 enyl) amine | |
| dc.subject | trifluoroacetic acid | |
| dc.subject | unclassified drug | |
| dc.subject | antibacterial activity | |
| dc.subject | article | |
| dc.subject | controlled study | |
| dc.subject | drug screening | |
| dc.subject | drug structure | |
| dc.subject | drug synthesis | |
| dc.subject | in vitro study | |
| dc.subject | minimum inhibitory concentration | |
| dc.subject | nonhuman | |
| dc.subject | X ray crystallography | |
| dc.title | A novel series of homoallylic amines as potential antimicrobials |
