Cargando…
β-Amino Esters from the Reductive Ring Opening of Aziridine-2-carboxylates
[Image: see text] A general study is undertaken to examine the scope of the reductive ring opening of aziridine-2-carboxylates with samarium diiodide. The competition between C–C and C–N bond cleavage is examined as a function of the nature of the N-substituent of the aziridine, the nature of the su...
Autores principales: | Zhao, Wenjun, Lu, Zhenjie, Wulff, William D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227569/ https://www.ncbi.nlm.nih.gov/pubmed/25329528 http://dx.doi.org/10.1021/jo501694h |
Ejemplares similares
-
Ammonium Salt‐Catalyzed Ring‐Opening of Aryl‐Aziridines with β‐Keto Esters
por: Haider, Victoria, et al.
Publicado: (2020) -
Efficient Regioselective Ring Opening of Activated Aziridine-2-Carboxylates with [(18)F]Fluoride
por: Schjoeth-Eskesen, Christina, et al.
Publicado: (2015) -
Unexplored Nucleophilic Ring Opening of Aziridines †
por: Costero, Ana María, et al.
Publicado: (2010) -
Alkylative Aziridine Ring-Opening Reactions
por: Choi, Jieun, et al.
Publicado: (2021) -
N-(1-Phenylethyl)aziridine-2-carboxylate esters in the synthesis of biologically relevant compounds
por: Głowacka, Iwona E, et al.
Publicado: (2019)