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- W3049126565 endingPage "131476" @default.
- W3049126565 startingPage "131476" @default.
- W3049126565 abstract "A novel and practical procedure for the preparation of α-amino secondary amides by the aminocarbonylation of N-Boc-imines using carbamoylsilanes bearing methoxymethyl group as secondary amides source is presented herein. The protocol tolerates N-Boc-imines bearing different groups, including aryl, double bond conjugated aryl, heteroaryl and aliphatic groups. The reactions provide good to excellent yields of the products under mild and catalysts-free conditions. The electronic property and the steric hindrance of substituent on the N-Boc-imines affect the reaction." @default.
- W3049126565 created "2020-08-21" @default.
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- W3049126565 date "2020-09-01" @default.
- W3049126565 modified "2023-10-13" @default.
- W3049126565 title "Efficient synthesis of α-amino secondary amides by direct aminocarbonylation of N-Boc-imines using carbamoylsilane as an amide source" @default.
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- W3049126565 doi "https://doi.org/10.1016/j.tet.2020.131476" @default.
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