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- W2898819093 endingPage "16731" @default.
- W2898819093 startingPage "16727" @default.
- W2898819093 abstract "Abstract Tertiary allylic alcohols equipped with a carboxyl group can be smoothly aminated under ambient conditions by a conceptually new and stereoselective protocol under palladium catalysis. The in situ formed Z‐configured γ‐amino acid cyclizes to afford an α,β‐unsaturated γ‐lactam, releasing water as the only byproduct. This practical catalytic transformation highlights the use of a carboxyl group acting as an activating and stereodirecting functional group to provide a wide series of pharma‐relevant building blocks. Various control reactions support the crucial role of the carboxyl group in the substrate to mediate these transformations." @default.
- W2898819093 created "2018-11-09" @default.
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- W2898819093 creator A5039315037 @default.
- W2898819093 creator A5065337367 @default.
- W2898819093 creator A5079438418 @default.
- W2898819093 date "2018-11-16" @default.
- W2898819093 modified "2023-10-18" @default.
- W2898819093 title "Domino Synthesis of α,β‐Unsaturated γ‐Lactams by Stereoselective Amination of α‐Tertiary Allylic Alcohols" @default.
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- W2898819093 doi "https://doi.org/10.1002/anie.201810160" @default.
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