scholarly journals Bay-Region-Selective Annulative π-Extension (APEX) of Perylene Diimides with Arynes

Synlett ◽  
2019 ◽  
Vol 30 (04) ◽  
pp. 423-428 ◽  
Author(s):  
Takayuki Nakamuro ◽  
Kazushi Kumazawa ◽  
Hideto Ito ◽  
Kenichiro Itami
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Short Axis ◽  
One Pot ◽  
Perylene Diimides ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

A bay-region-selective annulative π-extension (APEX) reaction of perylene diimides (PDIs) has been achieved by means of in-situ generated reactive aryne intermediates. This method provides an efficient one-pot π-extension at the short axis of PDIs in a sequential manner. Mechanistically, an inverse-electron-demand Diels–Alder reaction might be operative for the transformation.

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...

A silver-catalyzed domino inverse electron-demand oxo-Diels–Alder reaction of 3-cyclopropylideneprop-2-en-1-ones with 2,3-dioxopyrrolidines via cyclobutane-fused furan

2021 ◽  
Author(s):  
Yanshun Zhang ◽  
Yin Wei ◽  
Min Shi
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Tricyclic Compounds ◽  
Electron Demand

A silver-catalyzed diastereoselective domino cyclization-migration/inverse electron-demand oxo-Diels–Alder reaction of the in situ generated cyclobutane-fused furan intermediate with oxo-IED-diene for constructing complicated tricyclic compounds.

Site-specific one-pot triple click labeling for DNA and RNA

2018 ◽  
Vol 54 (83) ◽  
pp. 11781-11784 ◽  
Author(s):  
Marie-Luise Winz ◽  
Eva Christina Linder ◽  
Juliane Becker ◽  
Andres Jäschke
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
One Pot ◽  
Site Specific ◽  
Click Reactions ◽  
Inverse Electron Demand ◽  
Dna And Rna ◽  
Diels Alder Reaction ◽  
Electron Demand

We report site-specific triple click labeling for DNA and RNA in a one-pot setup by performing inverse electron demand Diels–Alder reaction and strain-promoted and copper catalyzed click reactions sequentially.

Sign in / Sign up

Export Citation Format

Share Document