Claisen rearrangement of 1-hydroxy-3-(3-methylbut-2-enyl)oxyxanthones
Abstract
Claisen rearrangement of three 1-hydroxy-3-(3-methylbut-2-enyl)oxyxanthones at 200° for 3 h yields the corresponding deprenylated xanthones and linear and angular furoxanthones, in contrast to previous results.