The regio-and stereoselective synthesis of cyclic iodo carbonates 1-10, resulting from allylic and homoallylic alcohols, was investigated. These useful intermediates were easily hydrolyzed to epoxy alcohols 11-20 or triols 21-30, depending on the polymeric reagent employed (Amberlyst A 26 in the OH-or C032-form, respectively). Stereochemical assignments were carried out by 13C NMR or'H NMR correlations and by conversion of ...
[Steinreiber, Andreas; Osprian, Ingrid; Mayer, Sandra F.; Orru, Romano V. A.; Faber, Kurt European Journal of Organic Chemistry, 2000 , # 22 p. 3703 - 3711]
[Steinreiber, Andreas; Osprian, Ingrid; Mayer, Sandra F.; Orru, Romano V. A.; Faber, Kurt European Journal of Organic Chemistry, 2000 , # 22 p. 3703 - 3711]