| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218477 | Tetrahedron | 2013 | 13 Pages |
Abstract
Arylated 1-methyl-1H-indoles were prepared by Suzuki–Miyaura cross-coupling reactions of 2,3-dibromo-1-methyl-1H-indole and 2,3,6-tribromo-1-methyl-1H-indole. The reactions proceed with very good regioselectivity in favour of position 2.
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