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Nguyen, ST; Zhu, QL; Knowles, RR in [Nguyen, Suong T.; Zhu, Qilei; Knowles, Robert R.] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA published PCET-Enabled Olefin Hydroamidation Reactions with N-Alkyl Amides in 2019.0, Cited 69.0. Recommanded Product: 1,1,1-Triethoxyethane. The Name is 1,1,1-Triethoxyethane. Through research, I have a further understanding and discovery of 78-39-7.

Olefin aminations are important synthetic technologies for the construction of aliphatic C-N bonds. Here we report a catalytic protocol for olefin hydroamidation that proceeds through transient amidyl radical intermediates that are formed via proton-coupled electron transfer (PCET) activation of the strong N-H bonds in N-alkyl amides by an excited-state iridium photocatalyst and a dialkyl phosphate base. This method exhibits a broad substrate scope, high functional group tolerance, and amenability to use in cascade polycyclization reactions. The feasibility of this PCET protocol in enabling the intermolecular anti-Markovnikov hydroamidation reactions of unactivated olefins is also demonstrated.

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