Charbonnet, Nicolas Riguet, Emmanuel Bochet, Christian G. 2011 Upon exposure to singlet oxygen and dimethylsulfide, the addition products between 3-furaldehydes and Grignard reagents undergo an oxidative rearrangement to give 2-substituted 3-furaldehydes, in yields ranging from 26-83%. N-Aryl- and N-tosylpyrroles were similarly obtained if the corresponding nitrogen-containing precursors were used instead, in equally attractive yields (64-92%). application/pdf https://folia.unifr.ch/global/documents/302343 https://folia.unifr.ch/documents/302343/files/boc_soi.pdf https://folia.unifr.ch/documents/302343/files/boc_soi_sm.pdf eng info:eu-repo/semantics/altIdentifier/doi/10.1055/s-0030-1261204 info:eu-repo/semantics/openAccess License undefined Synlett. - 2012, vol. 15, p. 2231-2233 Photochemistry Heterocycles Singlet oxygen Rearrangement Pyrroles Furans info:eu-repo/classification/udc/54 Singlet-Oxygen-Induced Rearrangement of Furan Derivatives http://purl.org/coar/resource_type/c_6501