| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224230 | Tetrahedron | 2008 | 5 Pages |
Abstract
An elegant one-pot synthesis of indenols was successfully realized starting from 3-aryl-2-bromopropenyl trifluoromethyl ketones and secondary amines. The synthesis proceeds through domino reactions including captodative aminoenones as a key intermediate. When bromoenones having a donor substituent in meta-position of the aromatic ring were subjected to this reaction, the mixture of two isomeric indenols was formed.
Graphical abstractDownload full-size image
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alexander Yu. Rulev, Igor A. Ushakov, Valentin G. Nenajdenko,