NEW METALATION AND SYNTHETIC APPLICATIONS OF ISONITRILES

被引:9
作者
ITO, Y
机构
[1] Department of Synthetic Chemistry, Kyoto University, Yoshida, Kyoto
关键词
D O I
10.1351/pac199062040583
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Insertions of isonitriles into silicon-tin linkage of organo-silylstannanes and silicon-silicon linkage of polysilanes are catalyzed by palladium complexes. [(N-2,6-xylylimino)trialkylsilylmethyl]stannanes thus prepared undergo transmetallation with n-butyllithium to generate in situ [(N-2,6-xylylimino)trialkylsilylmethyl]lithiums, which may serve as acyl anion equivalent in organic synthesis. Organozincs undergo the insertion reaction with aryl isocyanides to generate the correspondding α-(N-aryl-imino)alkylzincs, which may be synthetically used. Successive insertions of 1,2-diisocyanoarenes into Grignard reagent result in the formation of quinoxaline oligomers up to hexamer. © 1990, IUPAC.
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页码:583 / 588
页数:6
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