[Ir(3,4,7,8-Me4phen) (CH2CH2)2Cl]: A very active catalyst precursor for hydrogen transfer from alcohols to unsaturated organic substrates
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference10 articles.
1. Transfer of hydrogen from alcohols to ketones catalyzed by iridium complexes with 2,2′-bipyridine, 1,10-phenanthroline, and their derivatives
2. Enantioselective hydrogen transfers from isopropanol to prochiral ketones, using iridium complexes with nitrogen donor ligands as catalyst precursors
3. Chloro- and bromo-(alkene)iridium(I) complexes
4. Kinetic evidence for a possible end-on oxidative addition of dioxygen to a five-co-ordinate iridium(I) complex
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1. Polypyridyl iridium(III) based catalysts for highly chemoselective hydrogenation of aldehydes;Journal of Catalysis;2019-10
2. Enantioselective transfer hydrogenation of various ketones with novel efficient iridium(III) ferrocenyl-phosphinite catalysts;Journal of Organometallic Chemistry;2016-09
3. Highly efficient iridium catalysts based on C2-symmetric ferrocenyl phosphinite ligands for asymmetric transfer hydrogenations of aromatic ketones;Tetrahedron: Asymmetry;2015-12
4. {Ru–NO}6 and {Ru–NO}7 configurations in [Ru(trpy)(tmp)(NO)]n+ (trpy=2,2′:6′,2′′-terpyridine, tmp=3,4,7,8-tetramethyl-1,10-phenanthroline): An experimental and theoretical investigation;Inorganica Chimica Acta;2010-10
5. Asymmetric hydrosilylation, transfer hydrogenation and hydrogenation of ketones catalyzed by iridium complexes;Coordination Chemistry Reviews;2010-03
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