Preparation and transformations of acetophenone-derived enamino ketones, BF▫$_2$▫-▫$\beta$▫-ketoiminates, and BF▫$_2$▫-▫$\beta$▫-diketonatesBrodnik, Helena (Avtor) Ciber, Luka (Avtor) Grošelj, Uroš (Avtor) Petek, Nejc (Avtor) Štefane, Bogdan (Avtor) Svete, Jurij (Avtor) enaminonesketoiminatesdiketonatestransaminationphotochemistryDe Mayo reactionX-ray diffractionA series of differently substituted β-enaminones 2a,b, 4a–i, 8a–d, and 9–13, their BF$_2$-β-ketoiminate complexes 5a–d, and BF$_2$-β-diketonate complexes 6a–d were prepared as model substrates for photochemical transformations. The attempted photochemical transformations of enaminones 2, 4, 8 and BF$_2$-β-ketoiminate complexes 5 failed. On the other hand, irradiation of mixtures of BF$_2$-β-diketonate complexes 6a–d and cycloalkanes with UV-A light (365 nm) gave the corresponding De Mayo reaction products 7a–f in 9–30% yields. The photochemical ring-expansion of acetyl tetralone-derived BF$_2$-complex 6d gave novel diannulated cyclooctane derivatives 7e and 7f, which would be difficult to obtain using conventional cyclization methods.20252025-03-04 10:28:59Članek v reviji167609sl