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- W4255552904 endingPage "9658" @default.
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- W4255552904 abstract "Abstract An organocatalytic and highly regio‐, diastereo‐, and enantioselective intermolecular haloetherification and haloesterification reaction of allyl amides is reported. A variety of alkene substituents and substitution patterns are compatible with this chemistry. Notably, electronically unbiased alkene substrates exhibit exquisite regio‐ and diastereoselectivity for the title transformation. We also demonstrate that the same catalytic system can be used in both chlorination and bromination reactions of allyl amides with a variety of nucleophiles with little or no modification." @default.
- W4255552904 created "2022-05-12" @default.
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- W4255552904 date "2015-06-25" @default.
- W4255552904 modified "2023-10-18" @default.
- W4255552904 title "Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides" @default.
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- W4255552904 doi "https://doi.org/10.1002/ange.201502341" @default.
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