Abstract

We report in this paper the regioselective synthesis of functionalized oxime ethers 3 in good yields from the reaction of readily available starting material oximes with allyl bromides, derived from Baylis-Hillman adducts, in the presence of sodium hydride and triethyl amine under mild condition.

Keywords: Regioselective synthesis, Baylis-Hillman adduct, oxime, functionalized oxime ether