Demonstrates regioselective acylation of oxacorroles, indicating potential for new compound synthesis.
The Friedel–Crafts acylation of oxacorroles were performed by the reaction of 10-oxacorrole and acid chlorides in the presence of AlCl3, which give the 2-acylated-oxacorrole in moderate yields with regioselectivity. The structures of all the products were characterized by NMR, and HRMS analysis.
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Luo et al. (2026) studied this question.
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