Abstract
The mechanism of novel cyclization of 1, 3, 4-triacetoxy-2-acetylnaphthalene (I) to 2-methyl-3-acetyl-5-hydroxy-6-acetoxy-7, 8-benzochromone (II) was investigated by the 14Ctracer method and it was found that about 70∼80% of the reaction followed the route of (I)→(I')→(II).