par Baekelmans, Paul
;Gielen, Marcel
;Malfroid, P.;Nasielski, Jacques 
Référence Bulletin des Sociétés chimiques belges, 77, 1-2, page (85-97)
Publication Publié, 1968



Référence Bulletin des Sociétés chimiques belges, 77, 1-2, page (85-97)
Publication Publié, 1968
Article révisé par les pairs
Résumé : | The stereochemistry and the rate of the reaction of nine vinylic organotin compounds with iodine has been studied. A highly polar transition state A is suggested in order to interpret the reactivity sequences (1) and (2), the observed salt effect and the retention of configuration of the vinyl group. (Formula Presented.) Copyright © 1968 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim |