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- W2927582634 endingPage "2540" @default.
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- W2927582634 abstract "The first examples of electrochemical trifluoromethylation and sulfonylation/semipinacol rearrangements of allylic alcohols were developed using cheap and stable RSO2Na (R = CF3, Ph) as reagents. Various β-trifluoromethyl and sulfonated ketones were obtained in moderate to excellent yields. This strategy provides a facile, direct, and complementary approach to construct all-carbon quaternary stereocenters. In addition, the reaction has the advantages of being chemical oxidant-free and metal-free and has safe and mild reaction conditions." @default.
- W2927582634 created "2019-04-11" @default.
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- W2927582634 date "2019-04-04" @default.
- W2927582634 modified "2023-10-13" @default.
- W2927582634 title "Electrochemical Semipinacol Rearrangements of Allylic Alcohols: Construction of All-Carbon Quaternary Stereocenters" @default.
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- W2927582634 doi "https://doi.org/10.1021/acs.orglett.9b00263" @default.
- W2927582634 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30945551" @default.
- W2927582634 hasPublicationYear "2019" @default.
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