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Please use this identifier to cite or link to this item: http://hdl.handle.net/10481/47294

Title: Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates
Authors: Rodríguez Márquez, Irene
Milán Delgado, Alba
González Campaña, Araceli
Cuerva Carvajal, Juan Manuel
Issue Date: 14-Jan-2014
Abstract: 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.
Sponsorship: 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.
Publisher: Royal Society of Chemistry
Keywords: Intramolecular epoxide allylation
Allyl carbonates
Diastereoselective synthesis
URI: http://hdl.handle.net/10481/47294
ISSN: 2052-4129
Rights : Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License
Citation: 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]
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