Organometal additions to α-iminoesters:: N-alkylation via umpolung

被引:94
作者
Dickstein, Joshua S. [1 ]
Kozlowski, Marisa C. [1 ]
机构
[1] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
关键词
D O I
10.1039/b709139g
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
alpha-Iminoesters are useful precursors to substituted alpha-amino acid derivatives and are utilized in a number of organic transformations. As a consequence of the adjacent ester functionality, these imines are more reactive relative to other types of imines. While a significant body of work has focused on nucleophilic additions to the imine carbon (C-alkylation), a second pathway that involves nucleophilic reaction at the nitrogen (N-alkylation) is much less explored. This tutorial review highlights work that has exploited this unusual alpha-iminoester reactivity mode.
引用
收藏
页码:1166 / 1173
页数:8
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