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Collect. Czech. Chem. Commun. 1976, 41, 2714-2717
https://doi.org/10.1135/cccc19762714

Hyperconjugation in silaacenaphthenes

R. Ponec, E. A. Chernyshev, N. G. Tolstikova and V. Chvalovský

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  • Paquette Leo A., Hoppe Manfred, Johnston Linda J., Ingold Keith U.: Configurational characterization of the 1-(trimethylsilyl)cyclopropyl radical. Tetrahedron Letters 1986, 27, 411. <https://doi.org/10.1016/S0040-4039(00)85492-1>
  • Kiely John S., Boudjouk Philip: 1,8-Difunctionalized naphthalenes as building blocks. A convenient low temperature synthesis of 1-silaacenaphthenes. Journal of Organometallic Chemistry 1979, 182, 173. <https://doi.org/10.1016/S0022-328X(00)94380-8>
  • Adcock William, Aldous Graham L., Kitching William: The electronic effect of silyl substituents by 19F and 13C nmr : d-orbital participation versus hyperconjugation. Tetrahedron Letters 1978, 19, 3387. <https://doi.org/10.1016/S0040-4039(01)85648-3>
  • PONEC R., CHERNYSHEV E. A., TOLSTIKOVA N. G., CHVALOVSKY V.: ChemInform Abstract: ORGANOSILICON COMPOUNDS. CXLIII. HYPERCONJUGATION IN SILAACENAPHTHENES. Chemischer Informationsdienst 1977, 8. <https://doi.org/10.1002/chin.197701304>