1007382-76-4Relevant academic research and scientific papers
Enantioselective alkynylation to aldimines catalyzed by chiral 2,2′-di(2-aminoaryloxy)-1,1′-binaphthyl-copper(I) complexes
Hatano, Manabu,Asai, Takafumi,Ishihara, Kazuaki
, p. 379 - 382 (2008)
The enantioselective alkynylation of aldimines with terminal acetylenes catalyzed by chiral Cu(I) complexes with (R)-2,2′-di(2-aminoaryloxy)-1,1′-binaphthyl ligands (7) was examined. Chiral C2-symmetric N,N-ligands 7, which have primary aniline
Utilization of CO2 as a C1 Building Block in a Tandem Asymmetric A3 Coupling-Carboxylative Cyclization Sequence to 2-Oxazolidinones
Gao, Xiao-Tong,Gan, Chen-Chen,Liu, Si-Yue,Zhou, Feng,Wu, Hai-Hong,Zhou, Jian
, p. 8588 - 8593 (2017/12/08)
We report a tandem asymmetric aldehyde-alkyne-amine (A3) coupling-carboxylative cyclization sequence for the highly enantioselective synthesis of chiral N-aryl 2-oxazolidinones. This is a rare example of a multicatalyst-promoted asymmetric tand
Hydrogen-bonding asymmetric metal catalysis with α-amino acids: A simple and tunable approach to high enantioinduction
Lu, Yingdong,Johnstone, Tim C.,Arndtsen, Bruce A.
supporting information; experimental part, p. 11284 - 11285 (2011/03/21)
(Chemical Equation Presented) While asymmetric transition-metal catalysis has become a powerful method for constructing chiral products, a challenge in this field is the identification of the correct ligand for high selectivity. We report here a simple ap
