We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
Zwitterion‐Catalyzed Amino‐Dibromination of Nitroalkenes: Scope, Mechanism, and Application to The Synthesis of Glycinamides.
- Authors
Ng, Wing‐Hin; Lam, Ying‐Pong; Hu, Rong‐Bin; Ng, Wing‐Lok; Yeung, Ying‐Yeung
- 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.
- Subjects
NITROALKENES; BIOMOLECULES; NATURAL products
- Publication
Asian Journal of Organic Chemistry, 2021, Vol 10, Issue 5, p1131
- ISSN
2193-5807
- Publication type
Article
- DOI
10.1002/ajoc.202000514