Autor según el artículo: Echavarren, A.M.; Herlé, B.; Holstein, P.M.
Departamento: Química Analítica i Química Orgànica
Autor/es de la URV: ECHAVARREN PABLOS, ANTONIO MARIA; Herlé, B.; Holstein, P.M.
Palabras clave: cycloheptatrienes cyclopropanation Gold catalysis
Resumen: A highly stereoselective gold(I)-catalyzed cis-vinylcyclopropanation of alkenes has been developed. Allylic gold carbenes, generated via a retro-Buchner reaction of 7-alkenyl-1,3,5-cycloheptatrienes, react with alkenes to form vinylcyclopropanes. The gold(I)-catalyzed retro-Buchner reaction of these substrates proceeds by simple heating at a temperature much lower than that required for the reaction of 7-aryl-1,3,5-cycloheptatrienes (75 °C vs 120 °C). A newly developed Julia-Kocienski reagent enables the synthesis of the required cycloheptatriene derivatives in one step from readily available aldehydes or ketones. On the basis of mechanistic investigations, a stereochemical model for the cis selectivity was proposed. An unprecedented gold-catalyzed isomerization of cis- to trans-cyclopropanes has also been discovered and studied by DFT calculations.
Áreas temáticas: Química Química Chemistry
Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
ISSN: 2155-5435
Identificador del autor: 0000-0001-6808-3007; ;
Fecha de alta del registro: 2017-10-19
Página final: 3675
Volumen de revista: 7
Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
Enlace a la fuente original: http://pubs.acs.org/doi/abs/10.1021/acscatal.7b00737
Programa de financiación: euratom; European Research Council; ERC; 321066 european; MINECO/FEDER, UE; CTQ2016-75960-P MINECO-Severo Ochoa Excellence Acreditation 2014-2018; SEV; SEV-2013-0319 altres; Grups consolidats Generalitat de Catalunya; SGR; 2014 SGR 818
URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
DOI del artículo: 10.1021/acscatal.7b00737
Entidad: Universitat Rovira i Virgili
Año de publicación de la revista: 2017
Página inicial: 3668
Tipo de publicación: Article Artículo Article
Repositori URV