Switchable Catalysts Used To Control Suzuki Cross-Coupling and Aza–Michael Addition/Asymmetric Transfer Hydrogenation Cascade Reactions

ACS Catalysis ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 8693-8701 ◽  
Author(s):  
Jingjing Meng ◽  
Fengwei Chang ◽  
Yanchao Su ◽  
Rui Liu ◽  
Tanyu Cheng ◽  
...  
Keyword(s):  
Michael Addition ◽  
Cross Coupling ◽  
Cascade Reactions ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation

Facile assembly of bifunctional, magnetically retrievable mesoporous silica for enantioselective cascade reactions

2019 ◽  
Vol 55 (90) ◽  
pp. 13578-13581 ◽  
Author(s):  
Zhongrui Zhao ◽  
Fengwei Chang ◽  
Tao Wang ◽  
Lijian Wang ◽  
Lingbo Zhao ◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Cross Coupling ◽  
Bifunctional Catalyst ◽  
Cascade Reactions ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation ◽  
Aromatic Alcohols ◽  
Hydrogenation Reactions ◽  
Successive Reduction

A magnetically recyclable bifunctional catalyst enables synergistic Suzuki cross-coupling/asymmetric transfer hydrogenation and successive reduction/asymmetric transfer hydrogenation reactions for the preparation of chiral aromatic alcohols.

Enantioselective Dual-Catalysis: A Sequential Michael Addition/Asymmetric Transfer Hydrogenation of α-Nitrosulfone and Enones

ACS Catalysis ◽  
2020 ◽  
Vol 10 (18) ◽  
pp. 10381-10389
Author(s):  
Fengwei Chang ◽  
Shitong Wang ◽  
Zhitong Zhao ◽  
Lijian Wang ◽  
Tanyu Cheng ◽  
...  
Keyword(s):  
Michael Addition ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation ◽  
Dual Catalysis

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.

Enantioselectivity in the Noyori–Ikariya Asymmetric Transfer Hydrogenation of Ketones

2021 ◽  
Author(s):  
Pavel A. Dub ◽  
Nikolay V. Tkachenko ◽  
Vijyesh K. Vyas ◽  
Martin Wills ◽  
Justin S. Smith ◽  
...  
Keyword(s):  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation

Dendritic catalysts for asymmetric transfer hydrogenation based (1S,2R)-norephedrine derived ligands

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