Artículo
Double asymmetric hydrogenation of conjugated dienes: a self-breeding chirality route for C2 symmetric 1,4-diols
Autor/es | León García, Félix
Francos, Javier López Serrano, Joaquín García Garrido, Sergio E. Cadierno, Victorio Pizzano, Antonio |
Departamento | Universidad de Sevilla. Departamento de Química Inorgánica |
Fecha de publicación | 2019 |
Fecha de depósito | 2022-10-07 |
Publicado en |
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Resumen | The synthesis and double asymmetric hydrogenation of (Z,Z)-1,3-
diene-1,4-diyl diacetates is described. In this reaction C2/meso
ratios up to 85 : 15 and enantioselectivities up to 97% ee have been
achieved. As the ... The synthesis and double asymmetric hydrogenation of (Z,Z)-1,3- diene-1,4-diyl diacetates is described. In this reaction C2/meso ratios up to 85 : 15 and enantioselectivities up to 97% ee have been achieved. As the hydrogenation products can be converted into chiral 1,4-diols, key starting materials for the preparation of the best catalysts used, this catalytic system enables a self-breeding chirality process |
Agencias financiadoras | Ministerio de Economía y Competitividad (MINECO). España Agencia Estatal de Investigación. España European Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER) |
Identificador del proyecto | CTQ2016-75193-P
CTQ2016-75986-P CTQ2016-81797- REDC |
Cita | León García, F., Francos, J., López Serrano, J., García Garrido, S.E., Cadierno, V. y Pizzano, A. (2019). Double asymmetric hydrogenation of conjugated dienes: a self-breeding chirality route for C2 symmetric 1,4-diols. Chemical Communications, 55, 786-789. https://doi.org/10.1039/c8cc09391a. |
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Double asymmetric.pdf | 1.116Mb | [PDF] | Ver/ | Es versión aceptada del artículo publicado. |