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Turkish Journal of Chemistry, Vol.19, No.2, 73-79, 1995
SYNTHESIS OF SUBSTITUTED BENZOFURAN BY INTRAMOLECULAR [2+2] CYCLOADDITION REACTIONS OF PHENOXYKETENES TO CARBONYL GROUPS
Intramolecular [2+2] cycloaddition reactions of substituted o-formyl phenoxyketenes leading to substituted benzofurans have been identified. o-Formyl phenoxyketenes have been prepared in situ from alpha-(o-formyl phenoxy) carboxylic acids and then converted into benzofurans.