Studies in group IV organometallic chemistry XXIX. Mechanism of the hydrostannation of strongly electrophilic carbonyl compounds
article
The mechanism of the hydrostannation of strongly electrophilic carbonyl compounds has been studied. From the kinetics, and the solvent and substituent effects, it appears that the addition reaction proceeds by nucleophilic attack of the hydride hydrogen on carbon. Further aspects of this and secondary reactions are discussed. © 1968.
TNO Identifier
227044
ISSN
0022328X
Source
Journal of Organometallic Chemistry, 13(1), pp. 163-168.
Pages
163-168
Files
To receive the publication files, please send an e-mail request to TNO Repository.