Asymmetric transfer hydrogenation of ketones catalyzed by rhodium complexes containing amino acid triazole ligands

2010 ◽  
Vol 8 (20) ◽  
pp. 4536 ◽  
Author(s):  
Fredrik Tinnis ◽  
Hans Adolfsson
Keyword(s):  
Amino Acid ◽  
Transfer Hydrogenation ◽  
Rhodium Complexes ◽  
Asymmetric Transfer Hydrogenation

Asymmetric Transfer Hydrogenation of Ketones Catalyzed by Amino Acid Derived Rhodium Complexes: On the Origin of Enantioselectivity and Enantioswitchability

2009 ◽  
Vol 15 (42) ◽  
pp. 11197-11209 ◽  
Author(s):  
Katrin Ahlford ◽  
Jesper Ekström ◽  
Alexey B. Zaitsev ◽  
Per Ryberg ◽  
Lars Eriksson ◽  
...  
Keyword(s):  
Amino Acid ◽  
Transfer Hydrogenation ◽  
Rhodium Complexes ◽  
Asymmetric Transfer Hydrogenation

Theoretical Study of Asymmetric Transfer Hydrogenation of Ketones Catalyzed by Amino Acid-Derived Rhodium Complexes

ChemCatChem ◽  
2012 ◽  
Vol 4 (8) ◽  
pp. 1095-1104 ◽  
Author(s):  
Mikael Nordin ◽  
Rong-Zhen Liao ◽  
Katrin Ahlford ◽  
Hans Adolfsson ◽  
Fahmi Himo
Keyword(s):  
Amino Acid ◽  
Theoretical Study ◽  
Transfer Hydrogenation ◽  
Rhodium Complexes ◽  
Asymmetric Transfer Hydrogenation

scholarly journals Design of Iridium N-Heterocyclic Carbene Amino Acid Catalysts for Asymmetric Transfer Hydrogenation of Aryl Ketones

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 671
Author(s):  
Chad M. Bernier ◽  
Joseph S. Merola
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Enantiomeric Excess ◽  
Transfer Hydrogenation ◽  
Acid Catalysts ◽  
Asymmetric Transfer Hydrogenation ◽  
Reaction Conditions ◽  
Chiral Complexes ◽  
Acetophenone Derivatives ◽  
Aryl Ketones

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.

Third-Generation Amino Acid Furanoside-Based Ligands from d -Mannose for the Asymmetric Transfer Hydrogenation of Ketones: Catalysts with an Exceptionally Wide Substrate Scope

2016 ◽  
Vol 358 (24) ◽  
pp. 4006-4018 ◽  
Author(s):  
Jèssica Margalef ◽  
Tove Slagbrand ◽  
Fredrik Tinnis ◽  
Hans Adolfsson ◽  
Montserrat Diéguez ◽  
...  
Keyword(s):  
Amino Acid ◽  
Transfer Hydrogenation ◽  
Third Generation ◽  
Asymmetric Transfer Hydrogenation
Sign in / Sign up

Export Citation Format

Share Document