1,4-Dipolar cycloaddition in organic synthesis: A facile route to isoquinoline fused heterocycles

Abstract

The three component condensation reactions involving isoquinoline, dimethyl acetylenedicarboxylate and carbonyl dipolarophiles such as o- and p-benzoquinones and N-substituted isatins constitute a one-pot synthesis of a variety of [1,3]oxazino isoquinoline derivatives via 1,4-dipolar cycloaddition. © ARKAT.