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Photoaddition Reactions of Alkynes to Quinonoid Compounds

  • Kim Sung Sik (Department of Chemistry, ChonBuk National University) ;
  • Kim Ae Rhan (Department of Chemistry, ChonBuk National University) ;
  • Cho In Ho (Department of Chemistry, ChonBuk National University) ;
  • Shim Sang Chul (Department of Chemistry, Korea Advanced Institute of Science and Technology)
  • 발행 : 19890200

초록

UV irradiation of anthraquinone and diphenylacetylene in benzene gave 1:1 photoadduct (7) and cyclization product (8). The photoreaction of anthrone and diphenylacetylene in dichloromethane afforded the photooxidation products (7, 8, and 9) in air. The photoproduct (7) underwent the cyclization reaction during the purification by the column chromatography (silica gel). When irradiated with 350 nm UV light, the product (11) of benzil reacted with diphenylacetylene to give a photoadduct(12).

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참고문헌

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  14. Bull. Korean Chem. Soc. v.8 no.5 Sung Sik Kim;Yong Joon Yoon;In Ho Cho;Sang Chul Shim

피인용 문헌

  1. ChemInform Abstract: Photoaddition Reactions of Alkynes to Quinonoid Compounds. vol.20, pp.31, 1989, https://doi.org/10.1002/chin.198931072