Abstract
A 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.