1204591-61-6Relevant academic research and scientific papers
Self-association free bifunctional thiourea organocatalysts: Synthesis of chiral α-amino acids via dynamic kinetic resolution of racemic azlactones
Oh, Joong-Suk,Lee, Ji-Woong,Ryu, Tae Hee,Lee, Jae Heon,Song, Choong Eui
, p. 1052 - 1055 (2012/04/10)
Concentration-independent high enantioselectivity in the dynamic kinetic resolution (DKR) of racemic azlactones affording chiral α-aminoesters has been achieved using self-association free thiourea-based dimeric cinchona alkaloid organocatalysts. Detailed
Self-association-free dimeric cinchona alkaloid organocatalysts: Unprecedented catalytic activity, enantioselectivity and catalyst recyclability in dynamic kinetic resolution of racemic azlactones
Woong Lee, Ji,Hi Ryu, Tae,Suk Oh, Joong,Yong Bae, Han,Bin Jang, Hyeong,Eui Song, Choong
supporting information; scheme or table, p. 7224 - 7226 (2010/03/25)
Self-association-free, bifunctional, squaramide-based dimeric cinchona alkaloid organocatalysts show unprecedented catalytic activity, enantioselectivity and catalyst recyclability in the dynamic kinetic resolution (DKR) reaction of a broad range of racemic azlactones. The Royal Society of Chemistry 2009.
