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Collect. Czech. Chem. Commun. 1988, 53, 1745-1752
https://doi.org/10.1135/cccc19881745

Photochemistry of α-halocycloalkanones and α,α-dihalocycloalkanones. Ionic and radical photochemical carbon-halogen bond cleavage

Boris Šket and Marko Zupan

Department of Chemistry and J. Stefan Institute, E. Kardelj University of Ljubljana, Ljubljana, Yugoslavia

Crossref Cited-by Linking

  • Moon Da Yoon, An Sejin, Park Bong Ser: Synthesis of α,β-dibromo ketones by photolysis of α-bromo ketones with N-bromosuccinimide: Photoinduced β-bromination of α-bromo ketones. Tetrahedron 2019, 75, 130684. <https://doi.org/10.1016/j.tet.2019.130684>
  • An Sejin, Moon Da Yoon, Park Bong Ser: Solvent free, light induced 1,2-bromine shift reaction of α-bromo ketones. Tetrahedron 2018, 74, 6922. <https://doi.org/10.1016/j.tet.2018.10.015>
  • Jiménez M.Consuelo, Miranda Miguel A., Tormos Rosa: Influence of the intrazeolite microenvironment on the fate of the radical pairs formed by photolysis of 3-bromo-4-chromanone. J Photochem Photobiol A Chem 1995, 86, 225. <https://doi.org/10.1016/1010-6030(94)03948-T>
  • Kimura Takao, Kamewada Masaru, Kinoshita Jun, Minabe Masahiro: Photochemical Transformation of Telomers III. Photolysis of Dimethyl (2R*,4R*)-2-Bromo-2,4-dimethyl-4-(2,2,2-trichloroethyl)glutarate. Polym J 1994, 26, 1047. <https://doi.org/10.1295/polymj.26.1047>
  • Šket B., Zupančič N.: The photochemistry of 2-halo-1-tetralones. The effect of metal(II) salts and solid supports on the nature of carbon-halogen bond cleavage. J Photochem Photobiol A Chem 1992, 63, 303. <https://doi.org/10.1016/1010-6030(92)85195-Z>
  • Šket B., Zupančič N., Zupan M.: Photochemistry of α-fluorocycloalkanones and α-bromo- α- fluorocycloalkanones. J FLUORINE CHEM 1989, 45, 313. <https://doi.org/10.1016/S0022-1139(00)84156-1>