Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates
Identificadores
URI: http://hdl.handle.net/10481/47294DOI: 10.1039/C4QO00012A
ISSN: 2052-4129
ISSN: 2052-4110
Metadatos
Mostrar el registro completo del ítemAutor
Rodríguez Márquez, Irene; Milán Delgado, Alba; González Campaña, Araceli; Cuerva Carvajal, Juan ManuelEditorial
Royal Society of Chemistry
Materia
Intramolecular epoxide allylation Allyl carbonates Diastereoselective synthesis
Fecha
2014-01-14Referencia bibliográfica
Rodríguez Márquez, I.; et al. Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates. Organic Chemistry Frontiers, 4: 373-381 (2014). [http://hdl.handle.net/10481/47294]
Patrocinador
This research was funded by the Ministerio de Ciencia e Innovación (Spain) (project CTQ-2011.22455). I.R.M. thanks the MEC (Spain) for a predoctoral FPU fellowship. A.M. thanks the University of Granada for a postdoctoral contract (‘Contrato Puente’). A.G.C. thanks the MICINN (Spain) for a postdoctoral contract ‘Juan de la Cierva’ and University of Granada.Resumen
A useful method for the diastereoselective synthesis of vinyl substituted carbo- and heterocycles is described. Highly functionalized structures difficult to achieve by other methodologies are obtained in a single step by this procedure.