| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276097 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
A mild and efficient allylation/propargylation of indoles has been developed with high regioselectivity and excellent yields. In the presence of catalytic molecular iodine, various indoles could react with allylic/propargylic acetates smoothly at room temperature to exclusively provide C-3 alkylated products.
Graphical abstractA mild and efficient allylation/propargylation of indoles has been developed with high regioselectivities and excellent yields. In the presence of catalytic molecular iodine, various indoles could smoothly react with allylic/propargylic acetates at room temperature to exclusively provide C-3 alkylated products.Download full-size image
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhe Liu, Li Liu, Zahid Shafiq, Yan-Chao Wu, Dong Wang, Yong-Jun Chen,