Enantioselective Michael addition of 3(2H)-furanones to α,β-unsaturated aldehydes catalyzed by a diphenylprolinol silyl ether

2014 ◽  
Vol 55 (1) ◽  
pp. 209-211 ◽  
Author(s):  
Wujun He ◽  
Linhai Jing ◽  
Dabin Qin ◽  
Xiaohua Xie ◽  
Song Wu ◽  
...  
ChemInform ◽  
2014 ◽  
Vol 45 (21) ◽  
pp. no-no
Author(s):  
Wujun He ◽  
Linhai Jing ◽  
Dabin Qin ◽  
Xiaohua Xie ◽  
Song Wu ◽  
...  

2015 ◽  
Vol 51 (49) ◽  
pp. 9979-9982 ◽  
Author(s):  
Jin-Miao Tian ◽  
Yong-Hai Yuan ◽  
Yong-Qiang Tu ◽  
Fu-Min Zhang ◽  
Xiao-Bo Zhang ◽  
...  

A novel chiral spiro-pyrrolidine silyl ether organocatalyst has been designed and applied to an asymmetric Michael addition reaction.


Synthesis ◽  
2017 ◽  
Vol 49 (14) ◽  
pp. 3118-3125 ◽  
Author(s):  
Margus Lopp ◽  
Gert Preegel ◽  
Estelle Silm ◽  
Sandra Kaabel ◽  
Ivar Järving ◽  
...  

An asymmetric organocatalytic Michael addition–cyclization cascade reaction has been developed using cyclopentane-1,2-dione as a Michael donor and α,β-unsaturated aldehydes as Michael acceptors. Bicyclic hemiacetals were obtained in excellent yields and enantioselectivities. On the basis of the results, a one-pot reaction has been developed to obtain chiral 3-substituted cyclopentane-1,2-diones and substituted dihydropyrans in good yields and excellent enantioselectivity.


ChemInform ◽  
2011 ◽  
Vol 42 (33) ◽  
pp. no-no
Author(s):  
Wenjun Li ◽  
Wenbin Wu ◽  
Juanjuan Yang ◽  
Xinmiao Liang ◽  
Jinxing Ye

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