dc.date.accessioned | 2021-08-23T22:50:39Z | |
dc.date.accessioned | 2022-10-19T00:17:20Z | |
dc.date.available | 2021-08-23T22:50:39Z | |
dc.date.available | 2022-10-19T00:17:20Z | |
dc.date.created | 2021-08-23T22:50:39Z | |
dc.date.issued | 2017 | |
dc.identifier | http://hdl.handle.net/10533/250654 | |
dc.identifier | 1150712 | |
dc.identifier | WOS:000424424100003 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4481917 | |
dc.description.abstract | An amide chalconehas been synthesized in a two-step reaction. First, N-(4-acetylphenyl) quinoline-3-carboxamide 2 was synthesized by the reaction of quinoline-3-carboxylic acid 1 and thionyl chloride (SOCl2), following the addition of 4-aminoacetophenone. Then, a typical Claisen-Schmidtreactionwas made between 2 and piperonal using KOH solution as a catalystin ethanol, under ultrasonic irradiation. The structure of the target compound was established by FTIR (Fourier-transform infrared spectroscopy), HRMS, H-1 and C-13-NMR. | |
dc.language | eng | |
dc.relation | https://doi.org/10.3390/M960 | |
dc.relation | handle/10533/111557 | |
dc.relation | 10.3390/M960 | |
dc.relation | handle/10533/111541 | |
dc.relation | handle/10533/108045 | |
dc.rights | info:eu-repo/semantics/article | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Chile | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.title | N-{4-[(2E)-3-(2H-1,3-Benzodioxol-5-yl)prop-2-enoyl]phenyl}quinoline-3-carboxamide | |
dc.type | Articulo | |