过渡金属催化的成胍反应高效构建胍类衍生物
收稿日期: 2018-01-26
修回日期: 2018-02-14
网络出版日期: 2018-02-28
基金资助
国家自然科学基金(Nos.21725201,21572005)资助项目.
Transition-Metal-Catalyzed Guanylation Reaction of Amines with Carbodiimides Constructing Guanidines
Received date: 2018-01-26
Revised date: 2018-02-14
Online published: 2018-02-28
Supported by
Project supported by the National Natural Science Foundation of China (Nos. 21725201, 21572005).
王连军 , 迟樾 , 张文雄 , 席振峰 . 过渡金属催化的成胍反应高效构建胍类衍生物[J]. 有机化学, 2018 , 38(6) : 1341 -1349 . DOI: 10.6023/cjoc201801037
Guanidine derivatives are an important class of nitrogen-containing organic compounds, which are widely used in various pharmaceuticals, agrochemicals, sweeteners, explosives, and so on. Although classical methods for the synthesis of guanidines are established, there are still many fatal shortcomings which need to be resolved. In recent years, it has been gradually turned to the direct catalytic guanylation reaction of amines with carbodiimides. In this paper, the recent progress in transition-metal-catalyzed guanylation reaction of amines with carbodiimides to construct acyclic or cyclic guanidines based on the catalytic reaction mechanism, reaction system, the scope of substrates, etc. is reviewed.
Key words: guanylation reaction; guanidines; amines; carbodiimides
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