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Collect. Czech. Chem. Commun. 1989, 54, 3278-3283
https://doi.org/10.1135/cccc19893278

Radiation-initiated addition of acetaldehyde to allylalcohol and conversion of the 1:2-telomer into 1-methyl-2,8-dioxabicyclo[4,2,1]nonane

František Liška, Jiří Fikar, Petr Trška and Miroslav Valenta

Department of Organic Chemistry, Prague Institute of Chemical Technology, 166 28 Prague 6

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  • Taraban’ko V. E., Smirnova M. A., Zhizhina E. G.: Methods for the Synthesis of γ-Acetopropyl Alcohol. Catal. Ind. 2022, 14, 195. <https://doi.org/10.1134/S207005042202009X>
  • Tarabanko V. E., Smirnova M. A., Zhizhina E. G.: Processes for the synthesis of γ-acetopropyl alcohol. Kat.v.prom. 2022, 22, 5. <https://doi.org/10.18412/1816-0387-2022-2-5-17>
  • Liu Le-Ping, Hammond Gerald B.: Highly Efficient and Tunable Synthesis of Dioxabicyclo[4.2.1] Ketals and Tetrahydropyrans via Gold-Catalyzed Cycloisomerization of 2-Alkynyl-1,5-diols. Org. Lett. 2009, 11, 5090. <https://doi.org/10.1021/ol902215n>
  • Lucchesini Francesco, Bertini Vincenzo, Pocci Marco, Munno Giovanni De, Crispini Alessandra: New 2,3-dihydro-5h-1,4-benzodioxepin derivatives. Easy formation and x-ray structure determination of a pentacyclic acetal containing a fourteen-membered carbon-oxygen ring. Tetrahedron 1995, 51, 9757. <https://doi.org/10.1016/0040-4020(95)00583-T>
  • LISKA F., FIKAR J., TRSKA P., VALENTA M.: ChemInform Abstract: Radiation‐Initiated Addition of Acetaldehyde to Allyl Alcohol and Conversion of the 1:2‐Telomer into 1‐Methyl‐2,8‐dioxabicyclo(4,2,1)nonane. ChemInform 1990, 21. <https://doi.org/10.1002/chin.199013079>