Catalytic Asymmetric Tandem Reaction of Tertiary Enamides: Expeditious Synthesis of Pyrrolo[2,1-a ]isoquinoline Alkaloid Derivatives

2016 ◽  
Vol 128 (11) ◽  
pp. 3863-3867 ◽  
Author(s):  
Xin-Ming Xu ◽  
Liang Zhao ◽  
Jieping Zhu ◽  
Mei-Xiang Wang
2021 ◽  
Author(s):  
Wei Wu ◽  
Na Liao ◽  
Qi Wei ◽  
Jiaying Huang ◽  
Qi Huang ◽  
...  

2018 ◽  
Vol 54 (36) ◽  
pp. 4581-4584 ◽  
Author(s):  
Ming Yu Jin ◽  
Juncheng Li ◽  
Renke Huang ◽  
Yuxuan Zhou ◽  
Lung Wa Chung ◽  
...  

The tandem reaction realizes the asymmetric integration of –SCF3 group to carbonyl compounds, establishing the chiral tertiary α-carbon center and affording the α-SCF3-β-substituted carbonyl compounds in 50–92% yields with up to 20 : 1 dr and 96% ee.


2019 ◽  
Vol 58 (12) ◽  
pp. 4017-4021 ◽  
Author(s):  
Shulin Ge ◽  
Weidi Cao ◽  
Tengfei Kang ◽  
Bowen Hu ◽  
Hang Zhang ◽  
...  

2019 ◽  
Vol 131 (12) ◽  
pp. 4057-4061 ◽  
Author(s):  
Shulin Ge ◽  
Weidi Cao ◽  
Tengfei Kang ◽  
Bowen Hu ◽  
Hang Zhang ◽  
...  

2013 ◽  
Vol 9 ◽  
pp. 1210-1216 ◽  
Author(s):  
Jiahuan Peng ◽  
Da-Ming Du

The enantioselective tandem Friedel–Crafts alkylation/Michael addition reaction of indoles with nitroolefin enoates catalyzed by a diphenylamine-linked bis(oxazoline)-Zn(OTf)2 complex was investigated. This tandem reaction afforded functionalized chiral chromans in good yields with moderate to high stereoselectivities (up to 95:5 dr, up to 99% ee).


Author(s):  
Xin-Ming Xu ◽  
Ming Xie ◽  
Jiazhu Li ◽  
Mei-Xiang Wang

An exquisite Pybox/Cu(OTf)2-catalyzed asymmetric tandem reaction of tertiary enamides was developed, which enabled the expeditious synthesis of indolizino[8,7-b]indole derivatives in high yield, excellent enantioselectivity and diastereoselectivity.


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