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Copper/guanidine-catalyzed asymmetric alkynylation of isatin-derived ketimines
Chemical Communications ( IF 4.3 ) Pub Date : 2017-12-19 00:00:00 , DOI: 10.1039/c7cc08920a
Quangang Chen 1, 2, 3, 4, 5 , Lihua Xie 1, 2, 3, 4, 5 , Zhaojing Li 1, 2, 3, 4, 5 , Yu Tang 1, 2, 3, 4, 5 , Peng Zhao 1, 2, 3, 4, 5 , Lili Lin 1, 2, 3, 4, 5 , Xiaoming Feng 1, 2, 3, 4, 5 , Xiaohua Liu 1, 2, 3, 4, 5
Affiliation  

Isatin-derived ketimines undergo enantioselective alkynylation reactions in the presence of copper iodide and easily accessible guanidine-amides. The corresponding 3-alkynyl-3-aminooxyindoles are obtained in up to 95% yield and 96% ee. The guanidine plays a role in the formation of copper acetylide and the enantiodetermining step and the basic additive is excluded.

中文翻译:

铜/胍催化的伊斯兰衍生酮亚胺的不对称炔基化反应

伊斯兰衍生的酮亚胺在碘化铜和容易获得的胍酰胺存在下进行对映选择性炔基化反应。以高达95%的收率和96%的ee获得相应的3-炔基-3-氨基氧基吲哚。胍在乙炔铜的形成和对映体确定步骤中起作用,并且不包括碱性添加剂。
更新日期:2018-01-16
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