521937-32-6Relevant articles and documents
A facile route to pyrroles, isoindoles and hetero fused analogues
Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Pugh, Samantha L.
, p. 2799 - 2808 (2007/10/03)
The decarboxylative cyclisation process where enamino acids derived from 1, 2-dimethylaminomethylene or 1, 2 hydroxymethylene-carbonyl compounds and amino acids gets converted into pyrroles, isoindoles and other fused pyrroles, was discussed. The cyclisat
An unusual ring expansion from the Zav'yalov pyrrole synthesis: Formation of oxacino[2,3-c]pyrroles
Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Elsegood, Mark R. J.,Clegg, William
, p. 289 - 290 (2007/10/03)
Enamino acids 2 and 5 undergo a facile cyclisation to afford the pyrrole 3 and isoindole 6 ring systems; a novel two atom ring expansion ensues when derivatives 5b,d are subjected to the cyclisation conditions, resulting in the formation of the new oxacin
