Nucleophilic substitution products of Baylis–Hillman adducts are valuable synthons. In an attempt to improve the functionality of Baylis–Hillman adducts we report the regio- and chemo-selective fuctionalization of Baylis–Hillman bromides with symmetric and asymmetric bifunctional aromatics.
Nucleophilic substitution products of Morita–Baylis–Hillman adducts and their derivatives are valuable synthons. In an attempt to ameliorate the functionality of these functionalized motifs, we report the regio- and chemo-selective functionalization of Morita–Baylis–Hillman bromides with anthranilic acid.
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