950774-81-9Relevant articles and documents
Azavinyl azomethine ylides from thermal ring opening of α-aziridinohydrazones: Unprecedented 1,5-electrocyclization to imidazoles
Attanasi, Orazio A.,Davoli, Paolo,Favi, Gianfranco,Filippone, Paolino,Forni, Arrigo,Moscatelli, Giada,Prati, Fabio
, p. 3461 - 3464 (2008/02/12)
Michael-type addition of aziridinecarboxylates to 1,2-diaza-1,3-butadienes under solvent-free conditions (SFC) resulted in the formation of α-aziridinohydrazone adducts. In toluene under reflux, α-aziridinohydrazones gave imidazoles in moderate to good yi