A regioselective introduction of functional groups to the double bonds of allylic and homoallylic alcohols via the corresponding trichloroacetimidates

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Abstract
A new regioselective iodoamination reaction starting from allylic and homoallylic alcohols is described; the iodoaminoalcohols are obtained as the salts (2) and (4)via the corresponding 1,3-oxazolines (1) and dihydro-1,3-oxazines (3).