Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5286081 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Efficient modular synthetic routes to open chain marine alkaloids such as analogues of lamellarins have been developed. 5,6-Dihydropyrrolo[2,1-b]isoquinoline scaffolds were prepared, and protocols enabling regioselective bromination followed by Suzuki cross-coupling were established for the introduction of aryl groups onto the 2- and 3-positions.
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Authors
Christian A. Olsen, Núria Parera, Fernando Albericio, Mercedes Álvarez,