SnCl 2 mediated efficient N, N-dialkylation of azides to tertiary-amine via potential stannaimine intermediate
UK Roy, S Roy
Index: Roy, Ujjal Kanti; Roy, Sujit Journal of Organometallic Chemistry, 2006 , vol. 691, # 8 p. 1525 - 1530
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Citation Number: 3
Abstract
Under the aegis of anhydrous stannous chloride, the reaction of aliphatic or aromatic azides with organic halides (alkyl, benzyl, propargyl) lead to the formation of corresponding N,N-dialkylamines in good to excellent yields. Additional Pd(0) catalyst further enhances the yield in the case of
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