Dual C–H functionalization of N-aryl tetrahydroisoquinolines: a highly diastereoselective synthesis of dibenzo[a,f]quinolizines via visible-light induced oxidation and inverse electron-demand aza-Diels–Alder reaction

2016 ◽  
Vol 52 (6) ◽  
pp. 1190-1193 ◽  
Author(s):  
Guo-Qiang Xu ◽  
Chen-Guang Li ◽  
Ming-Qian Liu ◽  
Jian Cao ◽  
Yong-Chun Luo ◽  
...  

Dual C–H functionalization of amines with high diastereoselectivity is developedviavisible-light photocatalysis and inverse electron-demand aza-Diels–Alder reaction.

Author(s):  
Taotao Chen ◽  
Chao Che ◽  
Zhefei Guo ◽  
Xiu-Qin Dong ◽  
Chun-Jiang Wang

An unprecedented base-promoted and catalyst-free inverse-electron-demand aza-Diels-Alder (IEDDA) reaction between the easily available in situ generated azoalkenes and 3-vinylindoles has been developed. This efficient protocol afforded structurally important tetrahydropyridazines containing...


2017 ◽  
Vol 41 (21) ◽  
pp. 12392-12396 ◽  
Author(s):  
Siting Ni ◽  
Jun Zhu ◽  
Mohamed Amine Mezour ◽  
R. Bruce Lennox

A thermally-mild method for covalent binding of SWCNTs to AuNRs, based on an inverse-electron-demand Diels–Alder reaction, is established and discussed.


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