{"id":2236,"date":"2009-02-27T18:48:00","date_gmt":"2009-02-27T21:48:00","guid":{"rendered":"https:\/\/www.gluon.com.br\/blog\/?p=2236"},"modified":"2014-12-21T13:40:07","modified_gmt":"2014-12-21T13:40:07","slug":"dimetilaminopiridina-catalisador-nucleofilico","status":"publish","type":"post","link":"https:\/\/www.gluon.com.br\/blog\/2009\/02\/27\/dimetilaminopiridina-catalisador-nucleofilico\/","title":{"rendered":"Dimetilaminopiridina (catalisador nucleof\u00edlico)"},"content":{"rendered":"<p>O dimetilaminopiridina, ou DMAP, tem um uso geralmente em s\u00edntese org\u00e2nica como &#8220;catalisador nucleof\u00edlico&#8221;. O forte grupo doador dimetilamina proporciona sua nucleofilicidade.<br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.gluon.com.br\/blog\/wp-content\/uploads\/2009\/02\/dmap.gif\" alt=\"dmap molecula estrutura\" title=\"dmap\" width=\"164\" height=\"97\" class=\"alignnone size-full wp-image-2237\" \/><br \/>\nOs adutos formado pela adi\u00e7\u00e3o nucleof\u00edlica, contudo, s\u00e3o bastante reativos &#8211; an\u00e1logos a um \u00e1cido clor\u00eddrico &#8211; ent\u00e3o o DMAP pode for\u00e7ar bem a rea\u00e7\u00e3o. <a href=\"http:\/\/en.wikipedia.org\/wiki\/Dimethylaminopyridine\">Veja na Wikipedia<\/a> para entender o mecanismo.<\/p>\n<p><a href=\"http:\/\/scienceblogs.com\/moleculeoftheday\/2007\/07\/dimethylaminopyridine_nucleoph.php\">http:\/\/scienceblogs.com\/moleculeoftheday\/2007\/07\/dimethylaminopyridine_nucleoph.php<\/a><\/p>\n<p><small>Original (English) content from Molecule of the Day (<strong><a href=\"http:\/\/scienceblogs.com\/moleculeoftheday\">http:\/\/scienceblogs.com\/moleculeoftheday<\/a><\/strong>). Content translated with permission, but portuguese text not reviewed by the original author. Please do not distribute beyond this site without permission from both author and translator. <\/small><\/p>\n","protected":false},"excerpt":{"rendered":"<p>O dimetilaminopiridina, ou DMAP, tem um uso geralmente em s\u00edntese org\u00e2nica como &#8220;catalisador nucleof\u00edlico&#8221;. O forte grupo doador dimetilamina proporciona sua nucleofilicidade. Os adutos formado pela adi\u00e7\u00e3o nucleof\u00edlica, contudo, s\u00e3o bastante reativos &#8211; an\u00e1logos a um \u00e1cido clor\u00eddrico &#8211; ent\u00e3o o DMAP pode for\u00e7ar bem a rea\u00e7\u00e3o. Veja na Wikipedia para entender o mecanismo. http:\/\/scienceblogs.com\/moleculeoftheday\/2007\/07\/dimethylaminopyridine_nucleoph.php Original (English) content from Molecule of the Day (http:\/\/scienceblogs.com\/moleculeoftheday). Content translated with permission, but portuguese text not reviewed by the original author. Please do not distribute beyond this site without permission from both author and translator.<\/p>\n","protected":false},"author":1,"featured_media":5255,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[33],"tags":[],"class_list":["post-2236","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-mdd","has_thumb"],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO 4.9.9 - aioseo.com -->\n\t<meta name=\"description\" content=\"O dimetilaminopiridina, ou DMAP, tem um uso geralmente em s\u00edntese org\u00e2nica como &quot;catalisador nucleof\u00edlico&quot;. O forte grupo doador dimetilamina proporciona sua nucleofilicidade. Os adutos formado pela adi\u00e7\u00e3o nucleof\u00edlica, contudo, s\u00e3o bastante reativos - an\u00e1logos a um \u00e1cido clor\u00eddrico - ent\u00e3o o DMAP pode for\u00e7ar bem a rea\u00e7\u00e3o. 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