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Collect. Czech. Chem. Commun. 1971, 36, 925-928
https://doi.org/10.1135/cccc19710925

Quantitative studies in stereochemistry. XIV. Electrochemistry V. Effect of the medium on the stereochemistry of the electropinacolization of acetophenone

J. H. Stocker and R. M. Jenevein

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  • van Tilborg W. J. M., Smit C. J.: Asymmetric induction in electropinacolization. Recl. Trav. Chim. Pays-Bas 2010, 97, 89. <https://doi.org/10.1002/recl.19780970309>
  • van Tilborg W. J. M., Smit C. J.: The role of tetraalkylammonium salts in the electro-reduction of ketones III. Pinacolization and asymmetric induction. Recl. Trav. Chim. Pays-Bas 2010, 98, 532. <https://doi.org/10.1002/recl.19790981104>
  • Costentin Cyrille, Savéant Jean-Michel: Dimerization of electrochemically generated ion radicals: mechanisms and reactivity factors. Journal of Electroanalytical Chemistry 2004, 564, 99. <https://doi.org/10.1016/j.jelechem.2003.10.011>
  • Robertson Peter K. J., Eggins Brian R.: Photoelectrochemistry with quinone radical anions—photoassisted reduction of halobenzenes and carbonyl compounds. J. Chem. Soc., Perkin Trans. 2 1994, 1829. <https://doi.org/10.1039/P29940001829>
  • Gul'tyai V. P., Mendkovich A. S., Rubinskaya T. Ya.: Electrochemical hydrodimerization of carbonyl compounds in aprotic media. Russ Chem Bull 1987, 36, 1455. <https://doi.org/10.1007/BF01557522>
  • Gul'tyai V. P., Korotaeva L. M.: Role of medium components in the reactions of electrochemically generated radigal-anions 3. Stereochemistry and selectivity of the cathodic hydrodimerization of ?-thiophenaldehyde in nonaqueous media. Russ Chem Bull 1982, 31, 156. <https://doi.org/10.1007/BF00954428>
  • Belen'kii L. I., Gul'tyai V. P.: Redox transformations of compounds of the thiophene series (review). Chem Heterocycl Compd 1981, 17, 523. <https://doi.org/10.1007/BF00503474>
  • Gul'tyai V. P., Korotaeva L. M., Mendkovich A. S., Proskurovskaya I. V.: Role of components of the reaction medium in reactions of electrochemically generated radical anions. Russ Chem Bull 1981, 30, 615. <https://doi.org/10.1007/BF00949726>
  • van Tilborg W.J.M.: Phase‐sensitive detection of adsorption phenomena at a mercury electrode. Co‐adsorption of p‐bromoacetophenone and tetraethylammonium ions: (Preliminary communication). Recl. Trav. Chim. Pays‐Bas 1977, 96, 213. <https://doi.org/10.1002/recl.19770960710>
  • van Tilborg W.J.M., Smit C.J.: Electropinacolization; the role of tetraalkylammonium salts. Tetrahedron Letters 1977, 18, 3651. <https://doi.org/10.1016/S0040-4039(01)83317-7>
  • Juday Richard E., Waters William L.: The stereochemistry of the cathodic pinacolization of carbonyl compounds: The configuration of benzoin pinacol. Tetrahedron Letters 1975, 16, 4321. <https://doi.org/10.1016/S0040-4039(00)91113-4>
  • STOCKER J. H., JENEVEIN R. M.: ChemInform Abstract: QUANTITATIVE STEREOCHEMISCHE UNTERSUCHUNGEN 14. MITT. ELEKTROCHEMIE 5. MITT. EINFLUSS DES MEDIUMS AUF DIE STEREOCHEMIE DER ELEKTROPINAKOLISIERUNG VON ACETOPHENON. Chemischer Informationsdienst. Organische Chemie 1971, 2, no. <https://doi.org/10.1002/chin.197123133>