Journal
TETRAHEDRON-ASYMMETRY
Volume 26, Issue 15-16, Pages 769-790Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2015.06.016
Keywords
-
Funding
- Ministerio de Ciencia e Innovacion (MICINN) [CTQ2007-62771/BQU, CTQ2010-20387]
- Ministerio de Ciencia e Innovacion (MICINN) (CONSOLIDER INGENIO )
- Ministerio de Economia y Competitividad (MINECO) [CTQ2013-43446-P, CTQ2014-51912-REDC, CTQ2014-53695-P]
- FEDER
- Generalitat Valenciana [PROMETEO 2009/039, PROMETEOH/2014/017]
- University of Alicante
- CONSOLIDER INGENIO [2010-CDS2007-00006, CTQ2011-24151, CTQ2011-24165]
Ask authors/readers for more resources
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. (C) 2015 Elsevier Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available