1375488-95-1

Upstream product

• 21084-67-3 5,5′-(1,3-phenylene)bis(4-phenyl-4H-1,2,4-triazole-3-thiol) 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 1375488-98-4 2(1,3)-benzena-1⁽⁴⁾,3⁽⁴⁾-diphenyl-4,8-dithia-6-oxo-(1,3)(3,5)-1,2,4-triazolacyclooctaphane 

Relevant academic research and scientific papers

Novel synthesis of 1,2,4-triazolophanes and 1,3,4-oxadiazolophanes: A dieckmann condensation approach

The Dieckmann condensation has been used for the first time for the syntheses of novel 1,2,4-triazolophanes and 1,3,4-oxadiazolophanes. The bis-1,3,4-oxadiazol-2-thiols 1a and 1b were reacted with ethyl bromoacetate to give the diesters 2a and 2b. Diester