Marine Natural Meroterpenes: Synthesis and Antiproliferative Activity

Autor: Annabel Simon-Levert, Laurent Soulère, Anne Witczak, Anne-Marie Genevière, Chantal Barthomeuf, Bernard Banaigs, Christophe Menniti

Publikováno v: Marine Drugs, Vol 8, Iss 2, Pp 347-358 (2010)
Marine drugs
Marine drugs, MDPI, 2010, 8 (2), pp.347-358. ⟨10.3390/md8020347⟩
Marine Drugs; Volume 8; Issue 2; Pages: 347-358
Marine drugs, 2010, 8 (2), pp.347-358. ⟨10.3390/md8020347⟩
Marine Drugs

Meroterpenes are compounds of mixed biogenesis, isolated from plants, microorganisms and marine invertebrates. We have previously isolated and determined the structure for a series of meroterpenes extracted from the ascidian Aplidium aff. densum. Her

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1b440e83ca4efc6cabc1a706c00be0a
http://www.mdpi.com/1660-3397/8/2/347/

Rapid synthesis of methoxyconidiol and conitriol stereoisomers

Autor: Anne Witczak, Christophe Menniti, Bernard Banaigs, Nicolas Inguimbert, Gérald Lopez

Publikováno v: Tetrahedron Letters. 53:4548-4550

We describe the diastereoselective synthesis of the marine meroterpenes methoxyconidiol and conitriol in their trans form from the readily available 1-bromo-2,5-dimethoxybenzene in only three steps. The choice of the protective group strategy influen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e23f76eb4748dfa18d3a1e8e46e2a7de
https://doi.org/10.1016/j.tetlet.2012.06.050

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