摘要

The first sulfur ylides involved formal [5+1]-annulation reaction was developed between prop-2-ynylsulfonium salts and 2-(1H-indol-2-yl)phenols. Prop-2-ynylsulfonium salt participates in the reaction with its -carbon atom and acts as a novel C-1 synthon. Various indole-fused 4H-benzo[e][1,3]oxazines bearing a thioether moiety were constructed in good to high yields under mild conditions.