Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5284346 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Isomeric 1,5-, 1,6-, 1,7-, 2,6-, and 2,7-naphthalenediols react smoothly with benzene at room temperature in the presence of an excess of aluminum bromide to give 5-, 6-, and 7-hydroxy-4-phenyl-1-tetralones and 5- and 6-hydroxy-4-phenyl-2-tetralones, respectively.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Konstantin Yu. Koltunov,