Enantioselective Synthesis of Chromanones through Organocatalytic Tandem Reactions

2020 ◽  
Vol 362 (23) ◽  
pp. 5524-5528
Author(s):  
Mengxue Lu ◽  
Xin Wang ◽  
Zongli Xiong ◽  
Jingxiang Duan ◽  
Wen Ren ◽  
...  
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.


2020 ◽  
Vol 2 (10) ◽  
pp. 929-941
Author(s):  
Hong Je Cho ◽  
Bingjun Xu
Keyword(s):  

2018 ◽  
Author(s):  
Matthew L. Landry ◽  
Grace McKenna ◽  
Noah Burns

A concise and selective synthesis of the dichlorinated meroterpenoid azamerone is described. The paucity of tactics for the synthesis of chiral organochlorides motivated the development of unique strategies for accessing these motifs in enantioenriched forms. The route features a novel enantioselective chloroetherification reaction, a Pd-catalyzed cross-coupling between a quinone diazide and a boronic hemiester, and a late-stage tetrazine [4+2]-cycloaddition/oxidation cascade.


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