ChemInform Abstract: Highly Enantioselective Synthesis of Propargylic Alcohols by Way of the Asymmetric Aldol Reaction.

ChemInform ◽  
2010 ◽  
Vol 23 (9) ◽  
pp. no-no
Author(s):  
T. MUKAIYAMA ◽  
M. FURUYA ◽  
A. OHTSUBO ◽  
S. KOBAYASHI
1991 ◽  
Vol 20 (6) ◽  
pp. 989-992 ◽  
Author(s):  
Teruaki Mukaiyama ◽  
Minoru Furuya ◽  
Akihiro Ohtsubo ◽  
Shu Kobayashi

2016 ◽  
Vol 14 (1) ◽  
pp. 93-96 ◽  
Author(s):  
Allegra Franchino ◽  
Pavol Jakubec ◽  
Darren J. Dixon

A concise synthesis of (−)-chloramphenicol, based on the catalytic asymmetric aldol reaction between 4-nitrobenzaldehyde and benzhydryl isocyanoacetate, is reported.


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.


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