Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281243 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A process involving gold(I)-catalyzed formal carboamination of alkynes for the synthesis of C-3-substituted indoles has been developed. The procedure utilizes easily accessible starting materials such as 2-alkynylanilines and alkynols. A series of C-3-functionalized indoles are accessible by using this one-pot strategy. Mechanistically, the reaction involves three catalytic cycles and each of them is essentially catalyzed by a single metal catalyst, that is, Ph3PAuOTf.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Nitin T. Patil, Vipender Singh, Ashok Konala, Anil Kumar Mutyala,