Cargando…
Base-promoted highly efficient synthesis of nitrile-substituted cyclopropanes via Michael-initiated ring closure
A convenient and efficient annulation reaction has been developed for the general synthesis of dinitrile-substituted cyclopropanes in moderate to excellent yields. A variety of 2-arylacetonitriles and α-bromoennitriles were compatible under the standard conditions. The reaction was achieved through...
Autores principales: | Ye, Min, Xu, Fan, Bai, Yun, Zhang, Fanglian, Wang, Wenjia, Qian, Yiping, Chen, Zhengwang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536251/ https://www.ncbi.nlm.nih.gov/pubmed/36320497 http://dx.doi.org/10.1039/d2ra05393d |
Ejemplares similares
-
Structural Analysis of the Michael-Michael Ring Closure (MIMIRC) Reaction Products
por: Montenegro-Sustaita, Mabel M., et al.
Publicado: (2022) -
Synthesis of Trifluoroacetyl‐Substituted Cyclopropanes Using Onium Ylides
por: Winter, Michael, et al.
Publicado: (2018) -
Diastereoselective ring opening of fully-substituted cyclopropanes via intramolecular Friedel–Crafts alkylation
por: Lanke, Veeranjaneyulu, et al.
Publicado: (2019) -
Synthesis of Substituted 2-Benzoylaminothiobenzamides and Their Ring Closure to Substituted 2-Phenylquinazoline-4-thiones
por: Hanusek, Jiří, et al.
Publicado: (2001) -
Synthesis of highly substituted tetrahydroquinolines using ethyl cyanoacetate via aza-Michael–Michael addition
por: Palanimuthu, Arunan, et al.
Publicado: (2020)