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- W2151377346 abstract "Yes, nitrenes did “N,O”! Intermolecular addition of nitrene to enecarbamates and enesulfonamides gives oxyamidated products in excellent yields of up to 98 % and with good levels of stereoselectivity. Complete regioselectivity is also observed, leading to the formation of N,O-acetals which can further react with various nucleophiles under acidic conditions (see scheme; TcesNH2=trichloroethylsulfamate). Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2151377346 date "2011-12-08" @default.
- W2151377346 modified "2023-10-13" @default.
- W2151377346 title "Catalytic Selective Oxyamidation of Cyclic Enamides using Nitrenes" @default.
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- W2151377346 doi "https://doi.org/10.1002/chem.201102302" @default.
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