Direct Nucleophilic Substitution of Free Allylic Alcohols in Water Catalyzed by FeCl3⋅6 H2O: Which is the Real Catalyst?
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http://hdl.handle.net/10045/40229
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Campo DC | Valor | Idioma |
---|---|---|
dc.contributor | Síntesis Asimétrica (SINTAS) | es |
dc.contributor | Nuevos Materiales y Catalizadores (MATCAT) | es |
dc.contributor.author | Trillo Alarcón, María Paz | - |
dc.contributor.author | Baeza, Alejandro | - |
dc.contributor.author | Nájera, Carmen | - |
dc.contributor.other | Universidad de Alicante. Departamento de Química Orgánica | es |
dc.contributor.other | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica | es |
dc.date.accessioned | 2014-09-12T08:46:17Z | - |
dc.date.available | 2014-09-12T08:46:17Z | - |
dc.date.issued | 2013-06 | - |
dc.identifier.citation | ChemCatChem. 2013, 5(6): 1538-1542. doi:10.1002/cctc.201200650 | es |
dc.identifier.issn | 1867-3880 (Print) | - |
dc.identifier.issn | 1867-3899 (Online) | - |
dc.identifier.uri | http://hdl.handle.net/10045/40229 | - |
dc.description.abstract | The allylic substitution reaction, and particularly the direct allylic amination reaction, of free allylic alcohols in water catalyzed by FeCl3⋅6 H2O is described. This novel environmentally-friendly methodology allows the use of a wide variety of nitrogenated nucleophiles such as sulfonamides, carbamates, benzamides, anilines, benzotriazoles, and azides, generally giving good yields of the corresponding substitution products. The synthetic applicability of the process is also demonstrated because the reaction can be performed on gram-scale. Additionally, carbon nucleophiles such as silylated nucleophiles, aromatic compounds, and malonates also proved to be suitable for this transformation. Finally, the nature of the catalytic species present in aqueous media is unveiled, pointing towards the formation of hexaaquo iron(III) complexes. | es |
dc.description.sponsorship | Spanish Ministerio de Ciencia e Innovación (MICINN) (projects CTQ 2007-62771/BQU, CTQ2010-20387 and Consolider Ingenio 2010, CSD2007-00006), FEDER, the Generalitat Valenciana (PROMETEO 2009/039) and the University of Alicante are gratefully acknowledged for financial support. A.B. would like to thank MICINN for a Juan de la Cierva contract (JCI-2009-03710). | es |
dc.language | eng | es |
dc.publisher | Wiley-VCH Verlag GmbH & Co. KGaA | es |
dc.rights | © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim | es |
dc.subject | Allylic compounds | es |
dc.subject | Amination | es |
dc.subject | Green chemistry | es |
dc.subject | Iron | es |
dc.subject | Water chemistry | es |
dc.subject.other | Química Orgánica | es |
dc.title | Direct Nucleophilic Substitution of Free Allylic Alcohols in Water Catalyzed by FeCl3⋅6 H2O: Which is the Real Catalyst? | es |
dc.type | info:eu-repo/semantics/article | es |
dc.peerreviewed | si | es |
dc.identifier.doi | 10.1002/cctc.201200650 | - |
dc.relation.publisherversion | http://dx.doi.org/10.1002/cctc.201200650 | es |
dc.rights.accessRights | info:eu-repo/semantics/restrictedAccess | es |
Aparece en las colecciones: | INV - MATCAT - Artículos de Revistas INV - SINTAS - Artículos de Revistas INV - AMIC - Artículos de Revistas |
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2013_Trillo_etal_ChemCatChem_final.pdf | Versión final (acceso restringido) | 234,8 kB | Adobe PDF | Abrir Solicitar una copia |
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