Total Syntheses of the Actin??Binding Macrolides Latrunculin A, B, C, M, S and 16??epi??Latrunculin B
…, L Turet, MDB Fenster, L Parra??Rapado…
文献索引:Fuerstner, Alois; De Souza, Dominic; Turet, Laurent; Fenster, Michael D. B.; Parra-Rapado, Liliana; Wirtz, Conny; Mynott, Richard; Lehmann, Christian W. Chemistry - A European Journal, 2007 , vol. 13, # 1 p. 115 - 134
Abstract The latrunculins are highly selective actin-binding marine natural products and as such play an important role as probe molecules for chemical biology. A short, concise and largely catalysis-based approach to this family of bioactive macrolides is presented. Specifically, the macrocyclic skeletons of the targets were forged by ring-closing alkyne metathesis (RCAM) or enyne–yne metathesis of suitable diyne or enyne–yne precursors, ...
[Smith III, Amos B.; Leahy, James W.; Noda, Ichio; Remiszewski, Stacy W.; Liverton, Nigel J.; Zibuck, Regina Journal of the American Chemical Society, 1992 , vol. 114, # 8 p. 2995 - 3007]