Cargando…
Synthesis of bicyclo[3.1.0]hexanes by (3 + 2) annulation of cyclopropenes with aminocyclopropanes
We report the convergent synthesis of bicyclo[3.1.0]hexanes possessing an all-carbon quaternary center via a (3 + 2) annulation of cyclopropenes with cyclopropylanilines. Using an organic or an iridium photoredox catalyst and blue LED irradiation, good yields were obtained for a broad range of cyclo...
Autores principales: | Muriel, Bastian, Gagnebin, Alec, Waser, Jerome |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006509/ https://www.ncbi.nlm.nih.gov/pubmed/32110351 http://dx.doi.org/10.1039/c9sc03790j |
Ejemplares similares
-
Catalytic (3 + 2) annulation of donor–acceptor aminocyclopropane monoesters and indoles
por: Pirenne, Vincent, et al.
Publicado: (2021) -
Dearomatization of electron poor six-membered N-heterocycles through [3 + 2] annulation with aminocyclopropanes
por: Preindl, Johannes, et al.
Publicado: (2017) -
Synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexane via cyclopropene cycloadditions to the stable azomethine ylide derived from Ruhemann's purple
por: Filatov, Alexander S, et al.
Publicado: (2022) -
Synthesis and Evaluation of Bicyclo[3.1.0]hexane-Based UDP-Galf Analogues as Inhibitors of the Mycobacterial Galactofuranosyltransferase GlfT2
por: Lowary, Todd L., et al.
Publicado: (2016) -
Biological Evaluation of 3-Azaspiro[Bicyclo[3.1.0]Hexane-2,5′-Pyrimidines] as Potential Antitumor Agents
por: Shmakov, Stanislav V., et al.
Publicado: (2022)