Toward the racemic total synthesis of hederacines A and B: construction of an advanced tricyclic intermediate.

Toward the racemic total synthesis of hederacines A and B: construction of an advanced tricyclic intermediate.
复制标题

DOI:
10.1021/ol2004353
复制
发表时间:
2011-04
期刊:
影响因子:
5.2
通讯作者:
M. Yamashita;Tetsuya Yamashita;S. Aoyagi
M. Yamashita;Tetsuya Yamashita;S. Aoyagi
中科院分区:
化学1区
文献类型:
--
作者:
M. Yamashita;Tetsuya Yamashita;S. Aoyagi

文献摘要

相似文献

介绍了常春藤皂苷A和B的全合成研究进展。我们的方法包括烯丙基氰酸酯到异氰酸酯重排,烯炔闭环复分解,和C-5氨基和全氢甘菊环[5,6-B]呋喃酮中间体的C-12位之间的跨环反应。
Progress toward the total synthesis of hederacines A and B is described. Our approach involves an allylic cyanate-to-isocyanate rearrangement, eneyne ring-closing metathesis, and a transannular reaction between the C-5 amino group and the C-12 position of the perhydroazuleno[5,6-b]furanone intermediate.