Ruthenium-Catalyzed Tandem-Isomerization/Asymmetric Transfer Hydrogenation of Allylic Alcohols

2014 ◽  
Vol 20 (49) ◽  
pp. 16102-16106 ◽  
Author(s):  
Tove Slagbrand ◽  
Helena Lundberg ◽  
Hans Adolfsson
ChemInform ◽  
2015 ◽  
Vol 46 (28) ◽  
pp. no-no
Author(s):  
Christopher O. Shoola ◽  
Thomas DelMastro ◽  
Ruoqiu Wu ◽  
John R. Jr. Sowa

2015 ◽  
Vol 2015 (8) ◽  
pp. 1670-1673 ◽  
Author(s):  
Christopher O. Shoola ◽  
Thomas DelMastro ◽  
Ruoqiu Wu ◽  
John R. Sowa

2021 ◽  
Author(s):  
Kaili Zhang ◽  
Qixing Liu ◽  
Renke He ◽  
Danyi Chen ◽  
Zhangshuang Deng ◽  
...  

An asymmetric transfer hydrogenation of 2-arylidene four-, five-, six-, and seven-membered cycloalkanones under mild conditions has been performed. Various chiral exocyclic allylic alcohols were obtained by an exclusive reduction of CO bonds.


2019 ◽  
Vol 17 (2) ◽  
pp. 264-267 ◽  
Author(s):  
Sensheng Liu ◽  
Peng Cui ◽  
Juan Wang ◽  
Haifeng Zhou ◽  
Qixing Liu ◽  
...  

A chemoselective 1,2-reduction of cycloalkyl vinyl ketones to the corresponding chiral allylic alcohols via asymmetric transfer hydrogenation is described.


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 ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document