| dc.creator | Bustamante, Saúl E. | |
| dc.creator | Rivas, Bernabé L. | |
| dc.date | 2017-06-16 | |
| dc.date.accessioned | 2019-11-13T15:11:36Z | |
| dc.date.available | 2019-11-13T15:11:36Z | |
| dc.identifier | http://www.jcchems.com/index.php/JCCHEMS/article/view/205 | |
| dc.identifier.uri | https://revistaschilenas.uchile.cl/handle/2250/112612 | |
| dc.description | Methacrylic monomers with pyrylium salt derivatives are widely used to detect nucleophilic species. A new synthesis method has been used to obtain apyrylium salt that is trisubstituted with phenyl groups at positions 2,4, and 6. The phenyl group of the 4-position has a metacrylate group in the para-position. Thenew synthesis method implies the esterification of 4-hydroxybenzaldehyde, using methacrylic anhydride. The formed compound react with acetophenone to formthe pyrylium derivative. The yields of both reactions are greater than those previously reported in the literature. | en-US |
| dc.format | application/pdf | |
| dc.language | eng | |
| dc.publisher | Sociedad Chilena de Química | en-US |
| dc.relation | http://www.jcchems.com/index.php/JCCHEMS/article/view/205/166 | |
| dc.rights | Copyright (c) 2017 Saúl E. Bustamante, Bernabé L. Rivas | en-US |
| dc.rights | https://creativecommons.org/licenses/by-nc-sa/4.0 | en-US |
| dc.source | Journal of the Chilean Chemical Society; Vol 62 No 2 (2017): Journal of the Chilean Chemical Society | en-US |
| dc.source | 0717-9707 | |
| dc.source | 0717-9324 | |
| dc.title | NEW SYNTHESIS METHOD TO OBTAIN A METHACRYLIC MONOMER WITH A PYRYLIUM GROUP | en-US |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion | |
