Synthesis and absolute configuration assignment of albucidin: a late-stage reductive deiodination by visible light photocatalysis

2016 ◽  
Vol 14 (13) ◽  
pp. 3482-3485 ◽  
Author(s):  
Hu Zhang ◽  
Peng-Fei Liu ◽  
Qiong Chen ◽  
Qiong-You Wu ◽  
Anne Seville ◽  
...  

The total synthesis and absolute configuration assignment of albucidin might pave the way for synthetic and medicinal chemists for further research on this type of bioactive molecule.

2019 ◽  
Vol 131 (16) ◽  
pp. 5497-5500 ◽  
Author(s):  
Xiaogang Tong ◽  
Bingfei Shi ◽  
Kangjiang Liang ◽  
Qian Liu ◽  
Chengfeng Xia

2019 ◽  
Vol 58 (16) ◽  
pp. 5443-5446 ◽  
Author(s):  
Xiaogang Tong ◽  
Bingfei Shi ◽  
Kangjiang Liang ◽  
Qian Liu ◽  
Chengfeng Xia

2021 ◽  
Author(s):  
Shota Kato ◽  
Daichi Mizukami ◽  
Tomoya Sugai ◽  
Masashi Tsuda ◽  
Haruhiko Fuwa

An extensive application of cobalt-catalyzed Mukaiyama-type cyclization of γ-hydroxy olefins and a late-stage Stille-type reaction enabled syntheses of four diastereomers of amphirionin-2 to establish its absolute configuration.


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