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Collect. Czech. Chem. Commun. 1979, 44, 226-233
https://doi.org/10.1135/cccc19790226

Participation of the methoxyl group in the cleavage of some 19-substituted steroid epoxides. A case of competition between internal and external nucleophile attack

Pavel Kočovský and Václav Černý

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

Crossref Cited-by Linking

  • Ladika Mladen, Juršić Branko, Sunko Dionis E.: Solvolysis of 2-(ω-alkoxyalkyl)-3-methyl-2-cyclohexenyl p-nitrobenzoates. Tetrahedron 1987, 43, 179. <https://doi.org/10.1016/S0040-4020(01)89944-0>
  • Sicinski Rafal R., Szczepek Wojciech J.: Homoallylic rearrangement in the peracid oxidation of 19-iodo-5-androsten derivative. Tetrahedron Letters 1987, 28, 5729. <https://doi.org/10.1016/S0040-4039(00)96826-6>
  • Juršić Branko, Ladika Mladen, Sunko Dionis E.: Solvolysis of 2-(2-methoxyethyl)-3-methyl-2-cyclohexenyl p-nitrobenzoate. Tetrahedron 1986, 42, 911. <https://doi.org/10.1016/S0040-4020(01)87497-4>
  • KOCOVSKY P., CERNY V.: ChemInform Abstract: PARTICIPATION OF THE METHOXY GROUP IN THE CLEAVAGE OF SOME 19‐SUBSTITUTED STEROID EPOXIDES. A CASE OF COMPETITION BETWEEN INTERNAL AND EXTERNAL NUCLEOPHILE ATTACK. Chemischer Informationsdienst 1979, 10. <https://doi.org/10.1002/chin.197917345>