Dipartimento di Chimica, Università della Basilicata, Via N. Sauro 85, 85100, Potenza, Italy.
Photochem Photobiol Sci. 2010 Aug;9(8):1134-8. doi: 10.1039/c0pp00076k. Epub 2010 Jun 21.
The photochemical reaction of 2-substituted heterocyclic aldehydes with furan gave the corresponding exo oxetane derivatives through the excited triplet state. However, in situ the oxetane derivatives were converted through a metathesis reaction into the corresponding Z,E-butadienyl formate derivatives. On the contrary, 3-substituted heterocyclic aldehydes gave the corresponding exo oxetane derivatives. The effect of 2-substituted heterocyclic ring in order to facilitate the metathesis reaction is explained considering the possible participation of the pi aromatic orbitals in the oxetane C-O bond cleavage.
2-取代杂环醛与呋喃的光化学反应通过激发三重态生成相应的外消旋环氧乙烷衍生物。然而,在原位,通过复分解反应,这些环氧乙烷衍生物转化为相应的 Z,E-丁烯基甲酸酯衍生物。相反,3-取代杂环醛则生成相应的外消旋环氧乙烷衍生物。考虑到可能的芳环参与环氧乙烷 C-O 键的断裂,用 π 芳香轨道来解释 2-取代杂环环对促进复分解反应的影响。