85433-69-8Relevant academic research and scientific papers
COMPETING PATHWAYS IN THE PHOTODENITROGENATION OF A 3,5-DIHYDRO-4H-1,2,3-TRIAZOL-4-ONE. A NOVEL ROUTE TO AZIRIDINONES
Quast, Helmut,Seiferling, Bernhard
, p. 4681 - 4684 (1982)
The photodenitrogenation of the 3,5-dihydro-4H-1,2,3-triazol-4-one 6, obtained from 1-azidoadamantane (5) and the lithium enolate of methyl isobutyrate, produced acetone, the isocyanide 10 and the aziridinone 7, which was solvolysed to the α-methoxy amide 8 during photolysis in 4>methanol.
