A cinchona alkaloid catalyzed enantioselective sulfa-Michael/aldol cascade reaction of isoindigos: construction of chiral bispirooxindole tetrahydrothiophenes with vicinal quaternary spirocenters

2015 ◽  
Vol 13 (22) ◽  
pp. 6371-6379 ◽  
Author(s):  
Yong-Yuan Gui ◽  
Jian Yang ◽  
Liang-Wen Qi ◽  
Xiao Wang ◽  
Fang Tian ◽  
...  

Enantioselective sulfa-Michael/aldol reaction of isoindigos has been successfully developed to afford bispirooxindole tetrahydrothiophenes with vicinal quaternary spirocenters.

ChemInform ◽  
2011 ◽  
Vol 42 (37) ◽  
pp. no-no
Author(s):  
Pawel Czarnecki ◽  
Agnieszka Plutecka ◽  
Jacek Gawronski ◽  
Karol Kacprzak

2011 ◽  
Vol 13 (5) ◽  
pp. 1280 ◽  
Author(s):  
Paweł Czarnecki ◽  
Agnieszka Plutecka ◽  
Jacek Gawroński ◽  
Karol Kacprzak

2016 ◽  
Vol 14 (47) ◽  
pp. 11250-11260 ◽  
Author(s):  
Raghunath Chowdhury ◽  
Mukesh Kumar ◽  
Sunil K. Ghosh

Both enantiomers of functionalized 3,2′-pyrrolidinyl spirooxindoles were obtainedviaa Michael-cyclization cascade reaction using pseudoenantiomeric cinchona alkaloid derived thiourea based bifunctional catalysts.


Author(s):  
Xiqiang Hou ◽  
Jiang-Bo Wen ◽  
Li Yan ◽  
Da-Ming Du

A highly efficient cinchona alkaloid‐derived squaramide catalysed asymmetric Michael/cyclization cascade reaction of 4‐ arylmethylidene‐2,3‐dioxopyrrolidines with 2‐isothiocyanato‐1‐indanones was successfully developed. This protocol provides an efficient and mild access to obtain indanone‐derived...


2020 ◽  
Vol 18 (8) ◽  
pp. 1607-1611 ◽  
Author(s):  
Hongzhou Yang ◽  
Qingqing Wang ◽  
Yuan Luo ◽  
Ling Ye ◽  
Xinying Li ◽  
...  

An enantioselective Michael-initiated ring-closure process was established to construct β-CF3-cyclohexanones or β-CF3-cyclohexenones with cinchona alkaloid-based primary amines.


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