全合成
亚砜
化学
吲哚试验
立体化学
氧化磷酸化
核心
组合化学
有机化学
生物化学
生物
细胞生物学
作者
Scott D. Edmondson,Samuel J. Danishefsky
标识
DOI:10.1002/(sici)1521-3773(19980504)37:8<1138::aid-anie1138>3.0.co;2-n
摘要
Eight concise steps suffice for the first total synthesis of the title compound 1, which inhibits the transitions from the G2 and M phases into the next phases of the cell cycle. Key steps in the synthesis are a stereocontrolled oxidative rearrangement of an indole to form the chiral spiroindolinone nucleus and a regioselecitve sulfoxide elimination.
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