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- W4313232225 endingPage "251" @default.
- W4313232225 startingPage "243" @default.
- W4313232225 abstract "Although biomimetic or bioinspired synthesis is a widely used and powerful strategy for the efficient synthesis of naturally occurring molecules, prebiomimetic synthesis or prebioinspired organic synthesis has remained unprecedented. Herein, we report the first prebiomimetic synthesis of α-iminonitriles, N-monosubstituted and N,N-disubstituted α-cyanoenamines, and N-acyl derivatives from amides. The method is inspired by the possible prebiotic pathways put forward by Saladino/Di Mauro and Springsteen/Krishnamurthy–Leszczynski/Gu and features triflic anhydride (Tf2O)-mediated redox-neutral cyanation of secondary amides with trimethylsilyl cyanide (TMSCN) under mild conditions." @default.
- W4313232225 created "2023-01-06" @default.
- W4313232225 creator A5011550022 @default.
- W4313232225 creator A5014851609 @default.
- W4313232225 creator A5048553281 @default.
- W4313232225 creator A5063221338 @default.
- W4313232225 date "2022-12-28" @default.
- W4313232225 modified "2023-10-17" @default.
- W4313232225 title "Redox-Neutral Synthesis of α-Iminonitriles, α-Cyanoenamines, and <i>N</i>-Acyl Derivatives from Amides" @default.
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- W4313232225 doi "https://doi.org/10.1021/acsearthspacechem.2c00315" @default.
- W4313232225 hasPublicationYear "2022" @default.
- W4313232225 type Work @default.