Efficient Total Synthesis of Piceatannol via (E)-Selective Wittig–Horner Reaction

Abstract Efficient and practical total synthesis of piceatannol via (E)-selective Wittig–Horner reaction is demonstrated with six steps in overall 40% yield from a commercially available, cheap starting material, 3,5-dihydroxybenzoic acid. Wittig–Horner reaction of diethyl phosphonate with aldehyde showed a superior (E)-selectivity compare to Wittig reaction using triphenylphosphine. We optimized the Wittig–Horner reaction condition by using NaH (6 equiv) in tetrahydrofuran (THF) at reflux 1 h to give 99% yield of single (E)-stilbene.