Abstract
AbstractTetraalkyl‐methylendiamine (I) werden in Acetonitril oder Methylenchlorid bei ‐25° durch Nitronium‐tetrafluoroborat (II) zu Dialkyl‐nitraminen (III) nitriert; außerdem entstehen Dialkylaminomethylen‐tetrafluoroborate (IV).
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
