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• W2021012312 endingPage "4361" @default.
• W2021012312 startingPage "4358" @default.
• W2021012312 abstract "Redox-neutral formation of C–P bonds in the α-position of amines was achieved via a process that features a combination of an oxidative α-C–H bond functionalization and a reductive N-alkylation. Benzoic acid functions as an efficient catalyst in this three-component reaction of cyclic secondary amines, aldehydes and phosphine oxides to provide rapid access to α-amino phosphine oxides not easily accessible by classic Kabachnik–Fields reactions." @default.
• W2021012312 created "2016-06-24" @default.
• W2021012312 creator A5033182199 @default.
• W2021012312 creator A5083870648 @default.
• W2021012312 date "2013-08-19" @default.
• W2021012312 modified "2023-10-07" @default.
• W2021012312 title "Redox-Neutral α-C–H Bond Functionalization of Secondary Amines with Concurrent C–P Bond Formation/<i>N</i>-Alkylation" @default.
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• W2021012312 doi "https://doi.org/10.1021/ol401858k" @default.
• W2021012312 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3818705" @default.
• W2021012312 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23957378" @default.
• W2021012312 hasPublicationYear "2013" @default.
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