| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278174 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Suitably N-protected furoindolones react regioselectively with a variety of Michael acceptors in the presence of LDA to give 1-hydroxycarbazoles in a single-pot process and in good yields. The methodology has been applied to the synthesis of murrayafoline-A.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
D. Mal, B. Senapati, P. Pahari,
![First Page Preview: Regioselective synthesis of 1-hydroxycarbazoles via anionic [4+2] cycloaddition of furoindolones: a short synthesis of murrayafoline-A Regioselective synthesis of 1-hydroxycarbazoles via anionic [4+2] cycloaddition of furoindolones: a short synthesis of murrayafoline-A](/preview/png/5278174.png)