Catalytic asymmetric transfer hydrogenation of ketones: recent advances


Autoria(s): Foubelo, Francisco; Nájera Domingo, Carmen; Yus, Miguel
Contribuinte(s)

Universidad de Alicante. Departamento de Química Orgánica

Universidad de Alicante. Instituto Universitario de Síntesis Orgánica

Síntesis Asimétrica (SINTAS)

Data(s)

22/09/2016

22/09/2016

31/08/2015

Resumo

In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones from 2008 up today. The most effective organometallic compounds (derived from Ru, Rh, Ir, Fe, Os, Ni, Co, and Re) and chiral ligands (derived from amino alcohols, diamines, sulfur- and phosphorus-containing compounds, as well as heterocyclic systems) will be shown paying special attention to functionalized substrates, tandem reactions, processes under non-conventional conditions, supported catalysts, dynamic kinetic resolutions, the use of water as a green solvent, theoretical and experimental studies on reaction mechanisms, enzymatic processes, and finally applications to the total synthesis of biologically active organic molecules.

We thank the continuous financial support from our Ministerio de Ciencia e Innovación (MICINN) (projects CTQ2007-62771/BQU, CTQ2010-20387, CONSOLIDER INGENIO 2010-CDS2007-00006, CTQ2011-24151, CTQ2011-24165), the Ministerio de Economía y Competitividad (MINECO) (projects CTQ2013-43446-P, CTQ2014-51912-REDC, CTQ2014-53695-P), FEDER, the Generalitat Valenciana (PROMETEO 2009/039, PROMETEOII/2014/017), and the University of Alicante.

Identificador

Tetrahedron: Asymmetry. 2015, 26(15-16): 769-790. doi:10.1016/j.tetasy.2015.06.016

0957-4166 (Print)

1362-511X (Online)

http://hdl.handle.net/10045/58132

10.1016/j.tetasy.2015.06.016

Idioma(s)

eng

Publicador

Elsevier

Relação

http://dx.doi.org/10.1016/j.tetasy.2015.06.016

Direitos

© 2015 Elsevier Ltd.

info:eu-repo/semantics/embargoedAccess

Palavras-Chave #Catalysis #Asymmetric transfer hydrogenation #Ketones #Química Orgánica
Tipo

info:eu-repo/semantics/article