Asymmetric Synthesis of Both Mirror Images of 3′-Fluorothalidomide by Enantiodivergent Fluorination Using a Single, Cinchona Alkaloid

2011 ◽  
Vol 13 (3) ◽  
pp. 470-473 ◽  
Author(s):  
Takeshi Yamamoto ◽  
Yuka Suzuki ◽  
Emi Ito ◽  
Etsuko Tokunaga ◽  
Norio Shibata
Synfacts ◽  
2006 ◽  
Vol 2006 (8) ◽  
pp. 0841-0841
Author(s):  
L. Deng ◽  
F. Wu ◽  
R. Hong ◽  
J. Khan ◽  
X. Liu

2018 ◽  
Vol 16 (45) ◽  
pp. 8704-8709 ◽  
Author(s):  
Weihua Li ◽  
Yifeng Wang ◽  
Danqian Xu

A highly enantioselective nucleophilic addition of ketones to versatile imines catalyzed by chiral PTC has been developed, and the process affords the Mannich reaction products with tertiary stereocenters in good to high yields and excellent enantioselectivities. This protocol is effective for gram scale reaction.


ChemInform ◽  
2004 ◽  
Vol 35 (38) ◽  
Author(s):  
Alain Merschaert ◽  
Pieter Delbeke ◽  
Desire Daloze ◽  
Georges Dive

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2251 ◽  
Author(s):  
Xin Huang ◽  
Weizhao Zhao ◽  
Xiaofeng Zhang ◽  
Miao Liu ◽  
Stanley Vasconcelos ◽  
...  

A one-pot fluorination and organocatalytic Robinson annulation sequence has been developed for asymmetric synthesis of 6-fluoroyclohex-2-en-1-ones and 4,6-difluorocyclohex-2-en-1-ones. The reactions promoted by cinchona alkaloid amine afforded products bearing two or three stereocenters in good to excellent yields with up to 99% ee and 20:1 dr.


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