56601-90-2Relevant academic research and scientific papers
REACTIONS OF α-NITROALDAZINES WITH NUCLEOPHILIC REAGENTS
Nekrasova, G. V.,Lyamina, T. N.,Lipina, E. S.,Berkova, G. A.,Paperno, T. Ya.,et al.
, p. 794 - 797 (2007/10/02)
The reactions of the previously unknown α-nitroazines of aromatic aldehydes with aniline and sodium azide lead to derivatives of 1,2,4-triazole and tetrazole as a result of successive substitution of the nitro group and heterocyclization.
The Mechanism of Cyclization of 1,4-Diaryl-1-azido-2,3-diazabuta-1,3-dienes to Tetrazoles. Imidoyl Azides stabilized by Slow Nitrogen Inversion
Hegarty, Anthony F.,Brady, Kieran,Mullane, Maria
, p. 535 - 540 (2007/10/02)
The imidoyl azides (9) are stabilized in the open chain azido form because of their configuration (which is Z about the C=N bond) and slow ZE isomerization.The rates of conversion of the azides (9) into the isomeric tetrazoles (12) have been measused and
