Inverse substituent effect in an imidoyl azide to tetrazole cyclization limited by nitrogen inversion
Abstract
The azides (3) are stabilised in the open-chain form by a slow ZāE isomerisation about the C
N bond; electron-withdrawing substituents in Ar2 can either lower (by the operation of a mesomeric effect) or raise (by the inductive effect) this inversion barrier.
Please wait while we load your content...