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Development of a Benzimidazole‐Derived Bidentate P,N‐Ligand for Enantioselective Iridium‐Catalyzed Hydrogenations
Author(s) -
Weemers Jarno J. M.,
Sypaseuth Fanni D.,
Bäuerlein Patrick S.,
van der Graaff William N. P.,
Filot Ivo A. W.,
Lutz Martin,
Müller Christian
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201301243
Subject(s) - chemistry , enantioselective synthesis , ligand (biochemistry) , enantiomer , benzimidazole , denticity , stereochemistry , enantiomeric excess , imine , asymmetric hydrogenation , chiral ligand , catalysis , medicinal chemistry , combinatorial chemistry , organic chemistry , crystal structure , biochemistry , receptor
The development of a novel benzimidazole‐derived bidentate P,N‐ligand and its application in Ir‐catalyzed hydrogenation is described. The ligand backbone was obtained through a one‐pot tandem hydroformylation–cyclization sequence and the enantiomers of the generated alcohol were separated by chiral HPLC. By comparing the experimentally obtained CD spectra of the enantiomers with the simulated spectra generated from time‐dependent DFT calculations, the absolute configuration could be obtained. The chiral alcohols could further be isolated on a larger scale after transesterification by using Candida Antarctica lipase B (Novozym 435) and could subsequently be converted into the corresponding chiral P,N‐ligand by reaction with ClPPh 2 . The coordination properties of the racemic P,N‐ligand were investigated and the molecular structure of the Rh I complex [(P,N)Rh(CO)Cl] was determined by X‐ray crystal structure analysis. The corresponding chiral cationic Ir I complex was used as catalyst for the enantioselective hydrogenation of prochiral N ‐phenyl‐(1‐phenylethylidene)amine and trans ‐α‐methylstilbene. For the N ‐aryl‐substituted imine, enantiomeric excesses of only 10 % were obtained, whereas the unfunctionalized olefin could be hydrogenated with enantiomeric excesses of up to 90 %. Interestingly, the modular synthetic access to the P,N‐hybrid system described here allows facile modification of the ligand structure, which should extend the scope of such novel P,N‐ligands for asymmetric catalytic conversions to a large extent in the future.