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- W2936999937 abstract "We have developed a Rh(III)-catalyzed diastereoselective [2+1] annulation onto allylic alcohols initiated by alkenyl C-H activation of N-enoxyphthalimides to furnish substituted cyclopropyl-ketones. Notably, the traceless oxyphthalimide handle serves three functions: directing C-H activation, oxidation of Rh(III), and, collectively with the allylic alcohol, in directing cyclopropanation to control diastereoselectivity. Allylic alcohols are shown to be highly reactive olefin coupling partners leading to a directed diastereoselective cyclopropanation reaction, providing products not accessible by other routes." @default.
- W2936999937 created "2019-04-25" @default.
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- W2936999937 date "2019-04-18" @default.
- W2936999937 modified "2023-10-01" @default.
- W2936999937 title "Rh(III)-Catalyzed C–H Activation-Initiated Directed Cyclopropanation of Allylic Alcohols" @default.
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- W2936999937 doi "https://doi.org/10.1021/jacs.9b02156" @default.
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