Evans P Andrew, Delouvrié Bénédicte
Indiana University, Chemistry Department, 800 E Kirkwood Avenue, Bloomington, IN 47405, USA.
Curr Opin Drug Discov Devel. 2002 Nov;5(6):986-99.
The development of new synthetic methodology for the construction of trans-fused polycyclic ethers has stimulated significant attention since the late 1980s. This review provides an update on work reported between 2000 and 2002, emphasizing the development of iterative, convergent and cascade/two-directional cyclization strategies that provide direct and efficient approaches for the assembly of these complex structures. Recent developments in synthetic methodology have provided the tools necessary to accomplish the first total syntheses of ciguatoxin CTX3C and gambierol. Nonetheless, significant improvements in selectivity and versatility are clearly necessary for progress to be made in the construction of this class of molecules.
自20世纪80年代末以来,用于构建反式稠合多环醚的新合成方法的发展引起了广泛关注。本综述提供了2000年至2002年间报道工作的最新情况,重点强调了迭代、汇聚和级联/双向环化策略的发展,这些策略为组装这些复杂结构提供了直接而有效的方法。合成方法学的最新进展提供了完成西加毒素CTX3C和冈比甲藻毒素首次全合成所需的工具。尽管如此,要在这类分子的构建方面取得进展,选择性和通用性方面的显著改进显然是必要的。