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- W3139625112 abstract "A total synthesis of the biologically important diterpene ingenol has been completed. Ring-closing olefin metathesis was used to construct the strained “inside−outside” tetracyclic skeleton, and a series of diastereoselective reactions were employed to complete the synthesis. Another naturally occurring ingenane, 20-deoxyingenol, has also been prepared." @default.
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- W3139625112 date "2004-11-24" @default.
- W3139625112 modified "2023-09-26" @default.
- W3139625112 title "Total Synthesis of Ingenol" @default.
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- W3139625112 doi "https://doi.org/10.1021/ja044123l" @default.
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