An efficient and convenient 4 + 2 annulation between o-hydroxyphenyl-substituted p-quinone methides (p-QMs) and carbamates is developed for the construction of biologically useful benzoe1,3oxazin-2-ones. This novel strategy is distinguished by mild reaction conditions, simple operation, broad substrate scope, excellent yields, accessible scalability, and practical transformations.
Wang et al. (Sun,) studied this question.