A Metal-free Synthesis of N-Aryl Carbamates under Ambient Conditions

<p> <span style="color: rgb(51, 51, 51); font-family: 'Open Sans', Arial, Helvetica, 'Lucida Sans Unicode', sans-serif; font-size: 16px; font-style: normal; font-variant: normal; font-weight: normal; letter-spacing: normal; line-height: 24px; orphans: auto; text-ali...

Descripción completa

Detalles Bibliográficos
Autores: Guo, Wusheng, Gónzalez-Fabra, Joan, Bandeira, Nuno A. G., Bo, Carles, Kleij, Arjan W.
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2072/305762
Acceso en línea:http://hdl.handle.net/2072/305762
https://doi.org/10.1002/anie.201504956
Access Level:acceso abierto
Palabra clave:Carbon dioxide
N-aryl carbamates
organic carbonates
organocatalysis
site-specificity
Descripción
Sumario:<p> <span style="color: rgb(51, 51, 51); font-family: 'Open Sans', Arial, Helvetica, 'Lucida Sans Unicode', sans-serif; font-size: 16px; font-style: normal; font-variant: normal; font-weight: normal; letter-spacing: normal; line-height: 24px; orphans: auto; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; widows: 1; word-spacing: 0px; -webkit-text-stroke-width: 0px; display: inline !important; float: none; background-color: rgb(249, 249, 249);">The first chemo- and site-selective process for the formation of N-aryl-carbamates from cyclic organic carbonates and aromatic amines is reported. The reactions proceed smoothly under extremely mild reaction conditions using TBD (triazabicyclodecene) as an effective and cheap organocatalyst, thus providing a sustainable and new methodology for the formation of a wide variety of useful N-aryl carbamate synthons in good to excellent yields. Computational investigations have been performed and show the underlying reason for the observed unique reactivity as related to an effective proton-relay mechanism mediated by the bicyclic guanidine base.</span></p>