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- Publisher
- Wiley
- Copyright
- © 2021 Wiley‐VCH GmbH
- ISSN
- 2193-5807
- eISSN
- 2193-5815
- DOI
- 10.1002/ajoc.202000514
- Publisher site
- See Article on Publisher Site
Abstract
Glycinamides are valuable building blocks of natural products and biological relevant molecules. Many existing methods for the synthesis of glycinamides rely on harsh conditions. Herein, we report a zwitterion‐catalyzed aminobromination of nitroalkenes using N‐bromosuccinimide as the Br source and the amide donor. The resulting aminobromide products are converted into glycinamides.
Journal
Asian Journal of Organic Chemistry – Wiley
Published: May 1, 2021
Keywords: ; ; ; ;