Asymmetric hydrogen transfer reactions from propan-2-ol to ketones catalyzed by Ir(I) derivatives with chiral schiff bases
Author:
Publisher
Elsevier BV
Subject
General Engineering
Reference24 articles.
1. [Ir(3,4,7,8-Me4phen) (CH2CH2)2Cl]: A very active catalyst precursor for hydrogen transfer from alcohols to unsaturated organic substrates
2. Reduction of unhindered cyclohezxanones with propan-2-ol [Ir(3,4,7,8-Me4phen)HdI], an active and selective catalyst precursor
3. Selective reduction of α,β-unsaturated carbonyl compounds with alcohols catalyzed by ir(I) complexes containing 2,2'-bipyridine, 1,10-phenanthroline and substituted derivatives
4. Selective reduction of nitroaromatic compounds via hydrogen transfer, catalyzed by Ir(I) complexes with 2,2'-bipyridine, 1,10-phenanthroline and derivatives
5. Enantioselective transfer hydrogenation catalyzed by iridium(I) complexes with nitrogen donor ligands
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1. IrI(η4-diene) precatalyst activation by strong bases: formation of an anionic IrIII tetrahydride;Dalton Transactions;2023
2. Rhodium(I) bisaldimine complexes in transfer hydrogenation;Russian Journal of General Chemistry;2017-11
3. The cyclooctadiene ligand in [IrCl(COD)] 2 is hydrogenated under transfer hydrogenation conditions: A study in the presence of PPh 3 and a strong base in isopropanol;Journal of Organometallic Chemistry;2017-02
4. Ketone Hydrogenation with Iridium Complexes with “non N–H” Ligands: The Key Role of the Strong Base;ACS Catalysis;2015-06-18
5. Metal-complexes of optically active amino- and imino-based pyridine ligands in asymmetric catalysis;Coordination Chemistry Reviews;2013-06
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