Kashin, A. N. published the artcileReactivity of organotin compounds. XXVII. New method for the activation of organotin compounds in electrophilic substitution reactions. Study of the reaction kinetics of α-stannylated esters with iodine in the presence of triorganoiodostannanes, Synthetic Route of 31253-08-4, the publication is Zhurnal Organicheskoi Khimii (1984), 20(8), 1611-20, database is CAplus.
The kinetics of the reactions of R3SnCHR1CO2R2 (R = Me, Et, Bu; R1 = H, Me, Ph; R2 = Me, Et, Me2CH, Me3C) with iodine in DMF containing KI was studied. The reaction is autocatalytic with formation of R3SnI, and the final product is ICHR1CO2R2. In the presence of excess R3SnI the reaction is 2nd order overall, 1st order in each reactant, and its rate is not dependent on the KI and R3SnI concentrations
Zhurnal Organicheskoi Khimii published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C5H9IO2, Synthetic Route of 31253-08-4.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com