Simple one-pot preparations are described of chromanones, from phenoxy
propiononitriles via nucleophilic addition of an aryllithium to the ni
trile group and hydrolysis in situ of the formed azomethine, and xanth
ones, from diphenyl ethers via a metallation-CO2 reaction sequence; bo
th cyclizations are accomplished in a regiospecific manner and in the
presence of acid-sensitive groups.