Synthesis of a Biphenyl-Based Axially Chiral Amino Acid as a Highly Efficient Catalyst for the Direct Asymmetric Aldol Reaction.

ChemInform ◽  
2007 ◽  
Vol 38 (5) ◽  
Author(s):  
Taichi Kano ◽  
Osamu Tokuda ◽  
Keiji Maruoka
2005 ◽  
Vol 117 (20) ◽  
pp. 3115-3117 ◽  
Author(s):  
Taichi Kano ◽  
Jun Takai ◽  
Osamu Tokuda ◽  
Keiji Maruoka

ChemInform ◽  
2007 ◽  
Vol 38 (3) ◽  
Author(s):  
Xiaoping Tang ◽  
Benoit Liegault ◽  
Jean-Luc Renaud ◽  
Christian Bruneau

Tetrahedron ◽  
2016 ◽  
Vol 72 (13) ◽  
pp. 1706-1715 ◽  
Author(s):  
Pierre Milbeo ◽  
Kelly Maurent ◽  
Laure Moulat ◽  
Aurélien Lebrun ◽  
Claude Didierjean ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 648
Author(s):  
Yu-Hao Zhou ◽  
Yu-Zu Zhang ◽  
Zhu-Lian Wu ◽  
Tian Cai ◽  
Wei Wen ◽  
...  

A highly efficient quinine-derived primary-amine-catalyzed asymmetric aldol addition of hydroxyacetone to arylglyoxals is described. Structurally diverse anti-2,3-dihydroxy-1,4-diones were generated in high yields, with good diastereoselectivities and enantioselectivities.


ChemInform ◽  
2012 ◽  
Vol 43 (32) ◽  
pp. no-no
Author(s):  
Tsuyoshi Miura ◽  
Hikaru Kasuga ◽  
Kie Imai ◽  
Mariko Ina ◽  
Norihiro Tada ◽  
...  

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