Tetrahedron

Ring opening reactions of 1-arenesulfonyl-2-(bromomethyl) aziridines

M D'hooghe, I Kerkaert, M Rottiers, N De Kimpe

文献索引：D'Hooghe, Matthias; Kerkaert, Inge; Rottiers, Mario; De Kimpe, Norbert Tetrahedron, 2004 , vol. 60, # 16 p. 3637 - 3641

全文：HTML全文

被引用次数: 23

摘要

The reactivity of 1-arenesulfonyl-2-(bromomethyl) aziridines with respect to lithium dialkylcyanocuprates and lithium dialkylcuprates (Gilman reagents) has been evaluated for the first time, pointing to the conclusion that these substrates can be applied successfully as synthetic equivalents for the 2-aminopropane dication synthon towards 2-alkylaziridines and α-branched N-tosylamides in good yields.