Journal article

+ 1 other files

Singlet-Oxygen-Induced Rearrangement of Furan Derivatives

    2011
Published in:
  • Synlett. - 2012, vol. 15, p. 2231-2233
English 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%).
Faculty
Faculté des sciences et de médecine
Department
Département de Chimie
Language
  • English
Classification
Chemistry
License
License undefined
Identifiers
Persistent URL
https://folia.unifr.ch/unifr/documents/302343
Other files

Statistics

Document views: 7 File downloads:
  • boc_soi.pdf: 1
  • boc_soi_sm.pdf: 0