Artículos de revistas
Total Synthesis of Rutaecarpine and Analogues by Tandem Azido Reductive Cyclization Assisted by Microwave Irradiation
Registro en:
SYNLETT Issue: 1 Pages: 61-64 DOI: 10.1055/s-0030-1259095
0936-5214
Autor
Kamal, A.
Reddy, M.K.
Reddy, T.S.
Santos, L.S.
Shankaraiah, N.
Institución
Resumen
Santos, LS (Silva Santos, Leonardo). Univ Talca, Lab Asymmetr Synth, Chem Inst Nat Resources, Talca, Chile. The total synthesis of rutaecarpine and several analogues has been developed by using an azido reductive cyclization process starting from substituted azido benzoic acids. The intramolecular azido reductive cyclization step was performed with triphenylphosphine or Ni2B in HCl-MeOH (1 M) using microwave irradiation. This synthetic route is amenable for the generation of a library of quinazolinone compounds.