| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273708 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Reaction of electron-rich arenes with acetyl bromide and aldehydes in the presence of silica gel-supported zinc bromide was carried out in benzene to give selectively the corresponding triarylmethanes or 9,10-diarylanthracenes in high yields depending upon the ratio of an arene and an aldehyde. The mild conditions employed are especially noteworthy.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mitsuo Kodomari, Maki Nagamatsu, Megumi Akaike, Tadashi Aoyama,
