Catalyst-Free Aromatic Nucleophilic Substitution of meso-Bromoporphyrins with Azide Anion: Efficient Synthesis and Structural Analyses of meso-Azidoporphyrins

2011 ◽  
Vol 14 (1) ◽  
pp. 190-193 ◽  
Author(s):  
Ken-ichi Yamashita ◽  
Kazuyuki Kataoka ◽  
Motoko S. Asano ◽  
Ken-ichi Sugiura
Molecules ◽  
2018 ◽  
Vol 23 (10) ◽  
pp. 2576 ◽  
Author(s):  
Timofey Chmovzh ◽  
Ekaterina Knyazeva ◽  
Konstantin Lyssenko ◽  
Vadim Popov ◽  
Oleg Rakitin

A safe and efficient synthesis of 4,7-dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine from the commercial diaminomaleonitrile is reported. Conditions for selective aromatic nucleophilic substitution of one or two bromine atoms by oxygen and nitrogen nucleophiles are found, whereas thiols formed the bis-derivatives only. Buchwald-Hartwig or Ullmann techniques are successful for incorporation of a weak nitrogen base, such as carbazole, into the [1,2,5]thiadiazolo[3,4-d]pyridazine core. The formation of rather stable S…η2-(N=N) bound chains in 4,7-bis(alkylthio)-[1,2,5]thiadiazolo[3,4-d]pyridines makes these compounds promising for the design of liquid crystals.


Author(s):  
Xiaoyun Ran ◽  
Qian Zhou ◽  
Jin Zhang ◽  
Shanqiang Wang ◽  
Gui Wang ◽  
...  

Started from citric acid (CA) and ethylenediamine derivatives, a solvent-free, catalyst-free and highly yield synthesis approach for bicyclic 2-pyridones was presented. Continuing to modify the core structure, a series of...


Sign in / Sign up

Export Citation Format

Share Document