Results
1 -
2 of
2
(Click
here to explore results)
- Pentazole chemistry: the mechanism of the reaction of aryldiazonium chlorides with azide ion at –80 °C: concerted versus stepwise formation of arylpentazoles, detection of a pentazene intermediate, a combined 1H and 15N NMR experimental and ab initio theoretical study. Richard N. Butler, Anthony Fox, Seamus Collier, Luke A. Burke
, J. Chem. Soc., Perkin Trans. 2
, 1998
, 2243
- Synthesis of radiolabelled aryl azides from diazonium salts: experimental and computational results permit the identification of the preferred mechanism. Sameer M. Joshi, Abel de Cózar, Vanessa Gómez-Vallejo, Jacek Koziorowski, Jordi Llop, Fernando P. Cossío
, Chem. Commun.
, 2015
, 51
, 8954