“…The crude product obtained was purified by column chromatography (SiO 2 gel, hexanes−EtOAc 1:1, R f 0.60) to yield compound 11 (0.10 g, 8%) as a yellow liquid (which contained some methyl-5-formyl-2-methoxybenzoate that was removed in the next synthetic step): 1 H NMR (500 MHz, CDCl 3 , Figure S15) δ 8.45 (dd, J 1 = 2.3 Hz, J 2 = 0.5 Hz, 1H, aromatic), 8.08 (dd, J 1 = 9.1 Hz, J 2 = 2.3 Hz, 1H, aromatic), 7.68 (d, J = 2.4 Hz, 1H, aromatic), 7.34 (dd, J 1 = 8.6 Hz, J 2 = 2.5 Hz, 1H, aromatic), 7.29 (d, J = 9.1 Hz, 1H, aromatic), 6.90 (d, J = 8. 6…”