Skip to Content
Merck
  • Paternò-Büchi reaction between furan and heterocyclic aldehydes: oxetane formation vs. metathesis.

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

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology (2010-06-22)
Maurizio D'Auria, Rocco Racioppi, Licia Viggiani
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 pi aromatic orbitals in the oxetane C-O bond cleavage.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
3-Furancarboxaldehyde, ≥97%