Issue 8, 2010

Paternò–Büchi reaction between furan and heterocyclic aldehydes: oxetane formation vs.metathesis

Abstract

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 π aromatic orbitals in the oxetane C–O bond cleavage.

Graphical abstract: Paternò–Büchi reaction between furan and heterocyclic aldehydes: oxetane formation vs. metathesis

Article information

Article type
Paper
Submitted
26 Mar 2010
Accepted
07 Jun 2010
First published
21 Jun 2010

Photochem. Photobiol. Sci., 2010,9, 1134-1138

Paternò–Büchi reaction between furan and heterocyclic aldehydes: oxetane formation vs. metathesis

M. D'Auria, R. Racioppi and L. Viggiani, Photochem. Photobiol. Sci., 2010, 9, 1134 DOI: 10.1039/C0PP00076K

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