| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280677 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
The SmI3-catalyzed reaction of indoles with electron-deficient olefins generated the corresponding Michael adducts in high yields. The substitution on the indole nucleus occurred exclusively at the 3-position and N-alkylation products have not been observed.
Graphical abstractThe SmI3-catalyzed reaction of indoles with electron-deficient olefins generated the corresponding Michael adducts in high yields. The substitution on the indole nucleus occurred exclusively at the 3-position and N-alkylation products have not been observed.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhuang-Ping Zhan, Rui-Feng Yang, Kai Lang,