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- W4225281738 endingPage "1581" @default.
- W4225281738 startingPage "1575" @default.
- W4225281738 abstract "Abstract The synthesis of common cyclopropenes has been widely studied, but the synthesis of cyclopropenols is a significant challenge. Here, we highlight our recent work on the synthesis of trifluoromethylated cyclopropenols through a [2+1] cycloaddition reaction between alkynes and (trifluoroacetyl)silanes under visible-light-induced organocatalysis. The novel amphiphilic donor–acceptor carbenes derived from (trifluoroacetyl)silanes can react effectively with both activated and nonactivated alkynes. A broad substrate scope and a good functional-group tolerance have been achieved. Moreover, the synthetic potential of this reaction was highlighted by a gram-scale reaction and the one-pot diastereoselective synthesis of trifluoromethylated cyclopropanols." @default.
- W4225281738 created "2022-05-04" @default.
- W4225281738 creator A5016879516 @default.
- W4225281738 creator A5031890685 @default.
- W4225281738 date "2022-05-01" @default.
- W4225281738 modified "2023-10-16" @default.
- W4225281738 title "Visible-Light-Induced Organocatalyzed [2+1] Cyclization of Alkynes and (Trifluoroacetyl)silanes" @default.
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- W4225281738 doi "https://doi.org/10.1055/a-1840-5199" @default.
- W4225281738 hasPublicationYear "2022" @default.
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