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- W2091227006 abstract "Two syntheses of the tricyclic carbon skeleton of pleuromutilin are reported. Diastereoselective 1,4-conjugate additions were used to elaborate bicyclic precursors at an early stage of each route, while ring-forming olefin metatheses were executed to complete the pleuromutilin carbon framework. The congeners prepared are appropriately functionalized to enable access to diverse pleuromutilin analogues." @default.
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- W2091227006 date "2011-01-01" @default.
- W2091227006 modified "2023-10-18" @default.
- W2091227006 title "A concise synthesis of the molecular framework of pleuromutilin" @default.
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- W2091227006 doi "https://doi.org/10.1039/c0cc04077k" @default.
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