scholarly journals Does the Configuration at the Metal Matter in Noyori–Ikariya Type Asymmetric Transfer Hydrogenation Catalysts?

ACS Catalysis ◽  
2021 ◽  
pp. 13649-13659
Author(s):  
Andrew M. R. Hall ◽  
Daniel B. G. Berry ◽  
Jaime N. Crossley ◽  
Anna Codina ◽  
Ian Clegg ◽  
...  
2009 ◽  
Vol 15 (25) ◽  
pp. 6267-6278 ◽  
Author(s):  
Nicolas Vriamont ◽  
Bernadette Govaerts ◽  
Pierre Grenouillet ◽  
Claude de Bellefon ◽  
Olivier Riant

2012 ◽  
Vol 31 (8) ◽  
pp. 3333-3345 ◽  
Author(s):  
Daniel Carmona ◽  
Fernando J. Lahoz ◽  
Pilar García-Orduña ◽  
Luis A. Oro ◽  
M. Pilar Lamata ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 4076
Author(s):  
Vincent Ritleng ◽  
Johannes G. de Vries

In this review, we describe the synthesis and use in hydrogen transfer reactions of ruthenacycles and iridacycles. The review limits itself to metallacycles where a ligand is bound in bidentate fashion to either ruthenium or iridium via a carbon–metal sigma bond, as well as a dative bond from a heteroatom or an N-heterocyclic carbene. Pincer complexes fall outside the scope. Described are applications in (asymmetric) transfer hydrogenation of aldehydes, ketones, and imines, as well as reductive aminations. Oxidation reactions, i.e., classical Oppenauer oxidation, which is the reverse of transfer hydrogenation, as well as dehydrogenations and oxidations with oxygen, are described. Racemizations of alcohols and secondary amines are also catalyzed by ruthenacycles and iridacycles.


2015 ◽  
Vol 44 (27) ◽  
pp. 12119-12127 ◽  
Author(s):  
Paraskevi O. Lagaditis ◽  
Peter E. Sues ◽  
Alan J. Lough ◽  
Robert H. Morris

An iron ATH catalyst is slowly transformed into an inactive, achiral iron complex under catalytic conditions.


2015 ◽  
Vol 21 (22) ◽  
pp. 8043-8046 ◽  
Author(s):  
James P. C. Coverdale ◽  
Carlos Sanchez-Cano ◽  
Guy J. Clarkson ◽  
Rina Soni ◽  
Martin Wills ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 671
Author(s):  
Chad M. Bernier ◽  
Joseph S. Merola

A series of chiral complexes of the form Ir(NHC)2(aa)(H)(X) (NHC = N-heterocyclic carbene, aa = chelated amino acid, X = halide) was synthesized by oxidative addition of -amino acids to iridium(I) bis-NHC compounds and screened for asymmetric transfer hydrogenation of ketones. Following optimization of the reaction conditions, NHC, and amino acid ligands, high enantioselectivity was achieved when employing the Ir(IMe)2(l-Pro)(H)(I) catalyst (IMe = 1,3-dimethylimidazol-2-ylidene), which asymmetrically reduces a range of acetophenone derivatives in up to 95% enantiomeric excess.


Author(s):  
Pavel A. Dub ◽  
Nikolay V. Tkachenko ◽  
Vijyesh K. Vyas ◽  
Martin Wills ◽  
Justin S. Smith ◽  
...  

2003 ◽  
Vol 14 (16) ◽  
pp. 2481-2485 ◽  
Author(s):  
Pei Nian Liu ◽  
Ying Chun Chen ◽  
Xue Qiang Li ◽  
Yong Qiang Tu ◽  
Jin Gen Deng

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