2<i>H</i>-Chromenes from Salicylaldehydes by a Catalytic Petasis Reaction
2000-11-21T00:00:00Z (GMT) by
The Petasis condensation of vinylic or aromatic boronic acids, aromatic aldehydes, and amines is assisted by a hydroxy group adjacent to the aldehyde moiety. The products derived from salicylaldehydes and vinylboronic acids undergo cyclization to 2<i>H</i>-chromene compounds with ejection of amine upon heating. A catalytic preparation of 2<i>H</i>-chromenes using resin-bound amine is reported, allowing the convenient incorporation of a variety of components.