Abstract:Selective Substitution Reactions of Methoxycarbonylamino-1-(1-benzotriazolyl)alkanes with Active Methylene Compounds. -The leaving tendency of either methoxycarbonylamino or benzotriazole group by treatment of adducts (IV) with active methylene compounds (V) is studied. In the presence of the Lewis acid SmI3, -NH-E takes priority over -Btz in the leaving process, whereas -Btz is preferentially substituted in the presence of sodium methylate as base. In the first process, electron--withdrawing groups lead to ra… Show more
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