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- W4285193754 endingPage "9061" @default.
- W4285193754 startingPage "9056" @default.
- W4285193754 abstract "C(sp3)-H bond desaturation has been an attractive strategy in organic synthesis. Enamides are important structural fragments in pharmaceuticals and versatile synthons in organic synthesis. However, the dehydrogenation of amides usually occurs on the acyl side benefitting from enolate chemistry like the desaturation of ketones and esters. Herein, we demonstrate an Fe-assisted regioselective oxidative desaturation of amides, which provides an efficient approach to enamides and β-halogenated enamides." @default.
- W4285193754 created "2022-07-14" @default.
- W4285193754 creator A5018632765 @default.
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- W4285193754 creator A5081752937 @default.
- W4285193754 creator A5088430622 @default.
- W4285193754 creator A5090731919 @default.
- W4285193754 date "2022-01-01" @default.
- W4285193754 modified "2023-10-14" @default.
- W4285193754 title "Selective desaturation of amides: a direct approach to enamides" @default.
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