5,6-Dihydropyrrolo[2,1-b]isoquinolines as scaffolds for synthesis of lamellarin analogues
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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.
Originalsprog | Engelsk |
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Tidsskrift | Tetrahedron Letters |
Vol/bind | 46 |
Udgave nummer | 12 |
Sider (fra-til) | 2041-2044 |
Antal sider | 4 |
ISSN | 0040-4039 |
DOI | |
Status | Udgivet - 21 mar. 2005 |
ID: 240981481