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格氏试剂的两分子与硫代甲酰胺的顺序加成反应。

Sequential addition reactions of two molecules of Grignard reagents to thioformamides.

作者信息

Murai Toshiaki, Ui Kazuki

机构信息

Department of Chemistry, Gifu University, Yanagido, Gifu 501-1193, Japan.

出版信息

J Org Chem. 2009 Aug 7;74(15):5703-6. doi: 10.1021/jo900915n.

Abstract

Sequential addition reactions of two molecules of Grignard reagents to thioformamides were found to yield tertiary amines in an efficient manner. The addition of two different Grignard reagents can be accomplished by using one equivalent of arylmagnesium reagent in the first step. In the second step, a variety of reagents such as alkyl, alkenyl, aryl, and alkynyl reagents were used to afford the corresponding amines in good to high yields.

摘要

人们发现,格氏试剂的两个分子与硫代甲酰胺发生顺序加成反应能够高效地生成叔胺。通过在第一步使用一当量的芳基镁试剂,可以实现两种不同格氏试剂的加成。在第二步中,使用各种试剂,如烷基、烯基、芳基和炔基试剂,以良好至高收率得到相应的胺。

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