A novel one-pot synthesis of annulated 2,2′-bipyridine ligands by inverse electron demand Diels–Alder reaction of 5,5′-bi-1,2,4-triazines

2000 ◽  
Vol 41 (19) ◽  
pp. 3657-3659 ◽  
Author(s):  
Andrzej Rykowski ◽  
Danuta Branowska ◽  
Joanna Kielak
Synlett ◽  
2019 ◽  
Vol 30 (04) ◽  
pp. 423-428 ◽  
Author(s):  
Takayuki Nakamuro ◽  
Kazushi Kumazawa ◽  
Hideto Ito ◽  
Kenichiro Itami

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.


2018 ◽  
Vol 54 (83) ◽  
pp. 11781-11784 ◽  
Author(s):  
Marie-Luise Winz ◽  
Eva Christina Linder ◽  
Juliane Becker ◽  
Andres Jäschke

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.


2018 ◽  
Vol 54 (88) ◽  
pp. 12463-12466 ◽  
Author(s):  
C. T. Fathimath Salfeena ◽  
Basavaraja Basavaraja ◽  
K. T. Ashitha ◽  
V. Praveen Kumar ◽  
Sunil Varughese ◽  
...  

One-pot, scalable synthesis of symmetrical and unsymmetrical 2,4,6-triarylpyrylium ions via a highly regioselective inverse electron demand Diels–Alder (IEDDA) reaction.


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