117049-15-7Relevant articles and documents
Route of Triacylamine Formation in the Thermal Conversion of 2,3,7-Trioxa-5-azabicyclohept-5-enes Investigated by Nuclear Magnetic Resonance Experiments
Iesce, M. Rosaria,Graziano, M. Liliana,Cimminiello, Guido,Cermola, Flavio,Parrilli, Michelangelo,Scarpati, Rachele
, p. 1085 - 1089 (2007/10/02)
Thermal conversion of the typical aryl-, alkyl- and/or hydrogen-substituted oxazole endo-peroxides 2a-c into the triacylamines 5a-c proceeds by three subsequent rearrangements.The first leads to the dioxazoles 3a-c, which in the second stage rearrange into the imino anhydrides 4a-c.The latter collapse into the triacylamines 5a-c.