Orthogonal Synthesis of Isoindole and Isoquinoline Derivatives from Organic Azides
摘要:
alpha-Azido carbonyl compounds bearing a 2-alkenylaryl moiety at the alpha-position are found to be promising precursors for synthesis of isoindole and isoquinoline derivatives via 1,3-dipolar cycloaddition of azides onto alkenes and 6 pi-electrocyclization of N-H imine intermediates, respectively.
Orthogonal Synthesis of Isoindole and Isoquinoline Derivatives from Organic Azides
摘要:
alpha-Azido carbonyl compounds bearing a 2-alkenylaryl moiety at the alpha-position are found to be promising precursors for synthesis of isoindole and isoquinoline derivatives via 1,3-dipolar cycloaddition of azides onto alkenes and 6 pi-electrocyclization of N-H imine intermediates, respectively.