Triplet-sensitised di-π-methane rearrangement of N-substituted 2-azabarrelenones

Chem Commun (Camb). 2019 Jan 2;55(3):302-305. doi: 10.1039/c8cc08704k.

Abstract

When irradiated at λ = 366 nm or at λ = 420 nm in the presence of an appropriate sensitiser the title compounds underwent a di-π-methane rearrangement which led to the formation of tricyclic azasemibullvalenones (2a,2a1,2b,4a-tetrahydroazacyclopropa[cd]pentalenones) in yields of 63-87%.