α-Amino carbene or carbenoid formation in the reaction of a tertiary amide with PhMe2SiLi and its insertion into the Si-Li bond of a second equivalent

被引:26
作者
Fleming, I
Mack, SR
Clark, BP
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[2] Eli Lilly & Co, Lilly Res Ctr Ltd, Windlesham GU20 6PH, Surrey, England
关键词
D O I
10.1039/a800650d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
PhMe2SiLi reacts with tertiary amides, RCONMe2, to give a carbene, RCNMe2, or an equivalent carbenoid, which gives enediamines, R(Me2N) C=C (NMe2)R, in the absence of a strong nucleophile, but is attacked by strong nucleophiles, NuLi, to give lithium reagents R(Me2N)CLiNu.
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页码:713 / 714
页数:2
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