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- W4237078205 endingPage "11680" @default.
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- W4237078205 abstract "A new class of intermolecular olefin aminooxygenation reaction is described. This reaction utilizes the classic halonium intermediate as a regio- and stereochemical template to accomplish the selective oxyamination of both activated and unactivated alkenes. Notably, urea chemical feedstock can be directly introduced as the N and O source and a simple iodide salt can be utilized as the catalyst. This formal [3+2] cycloaddition process provides a highly modular entry to a range of useful heterocyclic products with excellent selectivity and functional-group tolerance." @default.
- W4237078205 created "2022-05-12" @default.
- W4237078205 creator A5004466545 @default.
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- W4237078205 creator A5041704012 @default.
- W4237078205 creator A5050229264 @default.
- W4237078205 creator A5084233429 @default.
- W4237078205 date "2019-07-17" @default.
- W4237078205 modified "2023-09-29" @default.
- W4237078205 title "Regioselective Formal [3+2] Cycloadditions of Urea Substrates with Activated and Unactivated Olefins for Intermolecular Olefin Aminooxygenation" @default.
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- W4237078205 doi "https://doi.org/10.1002/anie.201904662" @default.
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