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• W4307539554 abstract "The departure into unknown chemical space is essential for the discovery of new properties and function. We herein report the first synthetic access to N-trifluoromethylated formamides. The method involves the reduction of bench-stable NCF3 carbamoyl fluorides and is characterized by operational simplicity and mildness, tolerating a broad range of functional groups as well as stereocenters. The newly made N-CF3 formamide motif proved to be highly robust and compatible with diverse chemical transformations, underscoring its potential as building block in complex functional molecules." @default.
• W4307539554 created "2022-11-03" @default.
• W4307539554 creator A5047300640 @default.
• W4307539554 creator A5069167472 @default.
• W4307539554 creator A5089197606 @default.
• W4307539554 date "2022-11-23" @default.
• W4307539554 modified "2023-10-14" @default.
• W4307539554 title "Access to <i>N</i>−CF₃ Formamides by Reduction of <i>N</i>−CF₃ Carbamoyl Fluorides" @default.
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• W4307539554 doi "https://doi.org/10.1002/anie.202213829" @default.
• W4307539554 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36308723" @default.
• W4307539554 hasPublicationYear "2022" @default.
• W4307539554 type Work @default.
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• W4307539554 hasAuthorship W4307539554A5047300640 @default.

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