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- W2023362749 abstract "A combined inter-/intramolecular oxidative diamination of terminal alkenes is described that uses a hypervalent iodine oxidant and a nucleophilic amine to produce 3-aminoindolines at room temperature. This operationally straightforward and metal-free protocol is compatible with a broad range of functional groups. A mechanism involving the conversion of the amine to an electrophilic nitrogen source is advanced and used to identify a protocol effective with substoichiometric amounts of iodide and commercially available phenyl iodobenzene diacetate (PIDA) as the stoichiometric oxidant." @default.
- W2023362749 created "2016-06-24" @default.
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- W2023362749 date "2014-12-19" @default.
- W2023362749 modified "2023-09-27" @default.
- W2023362749 title "ChemInform Abstract: Alkene Diamination Using Electron-Rich Amines: Hypervalent Iodine-Promoted Inter-/Intramolecular C-N Bond Formation." @default.
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- W2023362749 doi "https://doi.org/10.1002/chin.201502119" @default.
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