摘要
平板霉素由于其强有力的抗菌能力、全新的作用机理和新颖的分子结构,自2006年被发现起就引起了合成化学家们的广泛关注.对平板霉素的全合成及其结构类似物的合成进行了综述和介绍.
Platensimycin represents a unique structural class of antibiotics acting with a novel and highly selective mechanism. Its potent antibacterial activity and interesting chemical structure have attracked great attention of scientific community, and have made it an attractive target for chemical synthesis. This review summarizes the total syntheses of platensimycin and its analogues since its discovery in 2006.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2008年第9期1553-1560,共8页
Chinese Journal of Organic Chemistry
关键词
平板霉素
抗生素
天然产物
四环笼状分子骨架
全合成
platensimycin
antibiotic
natural product
cage-like tetracyclic core
total synthesis