Collect. Czech. Chem. Commun.
1973, 38, 3496-3505
https://doi.org/10.1135/cccc19733496
Reactivity of compounds of diphenylmethane series. VI. Hydrolysis of benzhydryl bromides in 80% acetone; Cumulative effect of substituents
J. Mindl and M. Večeřa
Crossref Cited-by Linking
- Denegri Bernard, Streiter André, Jurić Sandra, Ofial Armin R., Kronja Olga, Mayr Herbert: Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale. Chemistry A European J 2006, 12, 1648. <https://doi.org/10.1002/chem.200500845>
- Hock Regina, Hillenbrand Stefanie, Erker Gerhard, Krüger Carl, Werner Stefan: Dihydroselenapyrans by [4 + 2] Cycloaddition of Diaryl Selenoketones. Chem. Ber. 1993, 126, 1895. <https://doi.org/10.1002/cber.19931260821>
- MINDL J., VECERA M.: ChemInform Abstract: REACTIVITY OF COMPOUNDS OF DIPHENYLMETHANE SERIES PART 6, HYDROLYSIS OF BENZHYDRYL BROMIDES IN 80 PERCENT ACETONE, CUMULATIVE EFFECT OF SUBSTITUENTS. Chemischer Informationsdienst 1974, 5. <https://doi.org/10.1002/chin.197408113>
