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  • alpha-Substituted o-alkylphenacyl derivatives were found to undergo photoinduced selective formation of the products in excellent chemical and moderate quantum yields. The reaction mechanism, studied by laser flash photolysis, was found to be largely dependent on the reaction conditions and the structure of the starting material. This procedure is suggested to be a facile synthetic route to some target skeletons, such as indanone, isobenzofuran, or methyleneindenone derivatives.
  • alpha-Substituted o-alkylphenacyl derivatives were found to undergo photoinduced selective formation of the products in excellent chemical and moderate quantum yields. The reaction mechanism, studied by laser flash photolysis, was found to be largely dependent on the reaction conditions and the structure of the starting material. This procedure is suggested to be a facile synthetic route to some target skeletons, such as indanone, isobenzofuran, or methyleneindenone derivatives. (en)
Title
  • The Photoenolization Reaction: Synthetic and Mechanistic Variations
  • The Photoenolization Reaction: Synthetic and Mechanistic Variations (en)
skos:prefLabel
  • The Photoenolization Reaction: Synthetic and Mechanistic Variations
  • The Photoenolization Reaction: Synthetic and Mechanistic Variations (en)
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  • RIV/00216224:14310/07:00020844!RIV11-GA0-14310___
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  • P(GA203/05/0641), Z(MSM0021622413)
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  • RIV/00216224:14310/07:00020844
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  • Photochemistry; photoenolization (en)
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  • [1D7D0936BA27]
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  • Klán, Petr
  • Plíštil, Lukáš
  • Tazhe Veetil, Aneesh
  • Literák, Jaromír
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  • 14310
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