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- W2016054232 abstract "Nickel(II) complex-catalyzed indirect electroreduction of N-allyl and N-propargyl-α-bromoamides conducted in dimethylformamide with 2 eq of a hydrogen atom donor, diphenylphosphine, afforded the corresponding pyrrolidinones as the sole cyclized product in good yields, while that of N-allyl-α-iodoamides in acetonitrile gave the iodinated pyrrolidinones. Under both conditions the trans-C-3: C-4 pyrrolidinones were formed predominantly" @default.
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- W2016054232 date "2010-08-17" @default.
- W2016054232 modified "2023-09-25" @default.
- W2016054232 title "ChemInform Abstract: Indirect Electroreductive Cyclization of N-Allyl and N-Propargylamides Using a Nickel(II) Complex as an Electron-Transfer Catalyst: Selective Formation of Halogenated and Non-Halogenated Pyrrolidinones." @default.
- W2016054232 cites W2952317795 @default.
- W2016054232 doi "https://doi.org/10.1002/chin.199531122" @default.
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