Synthesis of the marine sponge alkaloid oroidin and its analogues via Suzuki cross-coupling reactions
F Berrée, P Girard-Le Bleis, B Carboni
Index: Berree, Fabienne; Girard-Le Bleis, Pascale; Carboni, Bertrand Tetrahedron Letters, 2002 , vol. 43, # 28 p. 4935 - 4938
Full Text: HTML
Citation Number: 35
Abstract
Marine sponges are the source of the greatest diversity of marine natural products. Among these is the pyrrole–imidazole alkaloid family, where the common skeleton is observed in oroidin 1. 1 Various modes of cyclisation give rise to a large number of natural products with different geometries and functionalizations. Many of these compounds display a broad range of biological properties including antibacterial, antiinflammatory, anticancer and antiviral activities. ...
Related Articles:
[Jiang, Jinju; Chen, Xi; Feng, Jinhui; Wu, Qiaqing; Zhu, Dunming Journal of Molecular Catalysis B: Enzymatic, 2014 , vol. 100, p. 32 - 39]
Palladium-catalyzed synthesis of cinnamylamines
[Malek, Nancy J.; Moormann, Alan E. Journal of Organic Chemistry, 1982 , vol. 47, # 27 p. 5395 - 5397]