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- W2896572667 endingPage "18642" @default.
- W2896572667 startingPage "18638" @default.
- W2896572667 abstract "Iodocyclization of silyl group-substituted homopropargylic carbamates and amides proceeded via 6-exo-dig mode to afford 6-vinylene-4,5-dihydro-1,3-oxazines in moderate to quantitative yields. This is the first report for silyl group-solely directed iodocyclization of alkynes utilizing the β-silyl effect. Under these mild reaction conditions, various functionalities such as secondary alcohol, acetal, urea, and sulfide were tolerated." @default.
- W2896572667 created "2018-10-26" @default.
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- W2896572667 date "2018-11-26" @default.
- W2896572667 modified "2023-09-24" @default.
- W2896572667 title "Silyl Group‐Directed 6‐ <i>exo</i> ‐ <i>dig</i> Iodocyclization of Homopropargylic Carbamates and Amides" @default.
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- W2896572667 doi "https://doi.org/10.1002/chem.201804794" @default.
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