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Collect. Czech. Chem. Commun. 1979, 44, 110-122
https://doi.org/10.1135/cccc19790110

Mechanism of hydration and isomerisation of 4-ethylidene-2,6-di-tert-butyl-2,5-cyclohexadien-1-one. Kinetics, acid-base catalysis and solvent deuterium isotope effects

Jiří Velek, Bohumír Koutek and Milan Souček

Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6

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  • Zhou Qibing, Turnbull Kenneth D.: Quinone Methide Phosphodiester Alkylations under Aqueous Conditions. J. Org. Chem. 2001, 66, 7072. <https://doi.org/10.1021/jo015792+>
  • de la Mare Peter B.D., Newman Paul A.: Enhancement of the conjugative electron-releasing power of the hydroxy-group shown by the kinetics of solvolysis of 2-bromo-4-dibromomethylphenol and of 2-bromo-4-dibromomethyl-anisole. Tetrahedron Letters 1982, 23, 1305. <https://doi.org/10.1016/S0040-4039(00)87090-2>
  • VELEK J., KOUTEK B., SOUCEK M.: ChemInform Abstract: QUINONE METHIDES AND FUCHSONES. XIII. MECHANISM OF HYDRATION AND ISOMERIZATION OF 4‐ETHYLIDENE‐2,6‐DI‐TERT‐BUTYL‐2,5‐CYCLOHEXADIEN‐1‐ONE. KINETICS, ACID‐BASE CATALYSIS AND SOLVENT DEUTERIUM ISOTOPE EFFECTS. Chemischer Informationsdienst 1979, 10. <https://doi.org/10.1002/chin.197917185>