5,6-Dihydropyrrolo[2,1-b]isoquinolines as scaffolds for synthesis of lamellarin analogues
Research output: Contribution to journal › Journal article › Research › peer-review
Efficient modular synthetic routes to open chain marine alkaloids such as 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.
Original language | English |
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Journal | Tetrahedron Letters |
Volume | 46 |
Issue number | 12 |
Pages (from-to) | 2041-2044 |
Number of pages | 4 |
ISSN | 0040-4039 |
DOIs | |
Publication status | Published - 21 Mar 2005 |
- Cross-coupling reactions, Heterocycles, Marine alkaloids, Palladium
Research areas
ID: 240981481