| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5229380 | Tetrahedron | 2007 | 18 Pages |
Abstract
A simple route to 1-R-3-(2-indolyl)-1-propanones has been elaborated based on recyclization of 2-(2-aminobenzyl)furan derivatives. Being a modification of the Reissert indole synthesis, our approach employs the furan ring as a source of carbonyl function. This approach is general and allows varying of substituents in aromatic ring as well as in 3-position of indole nucleus.
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