作者:Susumu Ohira、Norihiro Fukamachi、Osamu Nakagawa、Masashi Yamada、Hiroshi Nozaki、Munekazu Iinuma
DOI:10.1246/cl.2000.464
日期:2000.5
Subelliptenone F, a potent inhibitor of topoisomerase II, was synthesized for the first time via coupling of A and C ring components and B ring formation, followed by Claisen rearrangement of the 3-methyl-2-butenyl ether.
亚椭圆酮F(Subelliptenone F),一种高效的拓扑异构酶II抑制剂,首次通过A环与C环成分的偶联以及B环的形成合成,随后进行3-甲基-2-丁烯基醚的克莱森重排。