The cleavage by iodine of the tin-tin bond in R6Sn2 compounds. Kinetics and mechanism

References

Page 1

	Year	Citations
Perfluoroalkyl Derivatives of Tin. I. Trimethyltrifluoromethyltin<sup>1</sup> H. C. Clark, C. J. Willis Journal of the American Chemical Society Derivative (Chemistry)Molecular SciencesDerivativesPerfluoroalkyl DerivativesEngineering	1960	101
316. Aromatic reactivity. Part X. Relative rates of cleavage of aryl–silicon, –tin, –germanium, and –lead bonds by aqueous-ethanolic perchloric acid Colin Eaborn, K. C. Pande Journal of the Chemical Society (Resumed) Materials ScienceAromatic ReactivityEngineeringNatural SciencesJ. Chem	1960	69
CHEMISTRY OF THE TRIMETHYLTIN GROUP Charles A. Kraus, William V. Sessions Journal of the American Chemical Society AltmetricsDerivative (Chemistry)EngineeringInformationDatabases	1925	69
Substitution Électrophile Aliphatique. Mécanisme et Vitesse de la Réaction D'Iododémétallation des Tétraméthyl, Éthyl, <i>n</i>PROPYL, <i>n</i>BUTYL et Allylétains M. Gielen, J. Nasielski Bulletin des Sociétés Chimiques Belges Chemical EngineeringSaturated Carbon AtomEngineeringBiochemistryChemical Transformation	1962	43
Assisted Acetolysis of Tributyltin Hydride Raymond E. Dessy, Thomas. Hieber, Frank E. Paulik Journal of the American Chemical Society AltmetricsBioorganic ChemistryEngineeringBiochemistryDonut Icon	1964	19
STUDIES RELATING TO ALKYL TIN COMPOUNDS. I. SOME STANNOETHANES. II. TRIMETHYLBENZYL STANNANE Charles A. Kraus, Ralph H. Bullard Journal of the American Chemical Society Materials ScienceTrimethylbenzyl StannaneMedicinal ChemistryChemical MeasurementEngineering	1926	17

Page 1