Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5266103 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
Al(OTf)3 catalyzed the alkylation of indoles using secondary/tertiary propargylic alcohols to produce 3-propargylated indoles in excellent yields with high selectivity. The reactions were performed in air with commercial grade solvents, and water was the only side product of the process. The catalyst was recovered after completion of the reaction and re-used with minimum loss of activity over three cycles.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mukut Gohain, Charlene Marais, Barend C.B. Bezuidenhoudt,