ChemInform Abstract: 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.

ChemInform ◽  
2016 ◽  
Vol 47 (20) ◽  
Author(s):  
Guo-Qiang Xu ◽  
Chen-Guang Li ◽  
Ming-Qian Liu ◽  
Jian Cao ◽  
Yong-Chun Luo ◽  
...  
Keyword(s):  
Visible Light ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diastereoselective Synthesis ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

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 ◽  
...  
Keyword(s):  
Visible Light ◽  
Alder Reaction ◽  
Diels Alder ◽  
Visible Light Photocatalysis ◽  
Diastereoselective Synthesis ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

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

Diastereoselective Synthesis of Functionalized Tetrahydropyridazines Containing Indole Scaffolds via Inverse-Electron-Demand Aza-Diels–Alder Reaction

2021 ◽  
Author(s):  
Taotao Chen ◽  
Chao Che ◽  
Zhefei Guo ◽  
Xiu-Qin Dong ◽  
Chun-Jiang Wang
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Diastereoselective Synthesis ◽  
Inverse Electron Demand ◽  
Catalyst Free ◽  
Diels Alder Reaction ◽  
Electron Demand

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...

Single wall carbon nanotube (SWCNT)–gold nanorod (AuNR) conjugates via thermally-mild reaction conditions

2017 ◽  
Vol 41 (21) ◽  
pp. 12392-12396 ◽  
Author(s):  
Siting Ni ◽  
Jun Zhu ◽  
Mohamed Amine Mezour ◽  
R. Bruce Lennox
Keyword(s):  
Carbon Nanotube ◽  
Covalent Binding ◽  
Alder Reaction ◽  
Diels Alder ◽  
Gold Nanorod ◽  
Reaction Conditions ◽  
Single Wall Carbon ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

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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