Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1327631 | Journal of Organometallic Chemistry | 2009 | 5 Pages |
Abstract
Reaction of a monosubstituted, 1,3-disubstituted, or tetrasubstituted allene with various indoles catalyzed by a 1:1 mixture of a gold(I) N-heterocyclic carbene complex and AgOTf at room temperature leads to hydroarylation with formation of 3-allyl-indoles in modest to good yield.
Graphical abstractReaction of monosubstituted, 1,3-disubstituted, or tetrasubstituted allenes with an indole in the presence of a catalytic 1:1 mixture of a gold(I) N-heterocyclic carbene complex and AgOTf at room temperature leads to hydroarylation with formation of 3-allyl-1,2-dimethylindoles in modest to good yield.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Kristina L. Toups, Gordon T. Liu, Ross A. Widenhoefer,