Cargando…
Radical asymmetric intramolecular α-cyclopropanation of aldehydes towards bicyclo[3.1.0]hexanes containing vicinal all-carbon quaternary stereocenters
The development of a general catalytic method for the direct and stereoselective construction of cyclopropanes bearing highly congested vicinal all-carbon quaternary stereocenters remains a formidable challenge in chemical synthesis. Here, we report an intramolecular radical cyclopropanation of unac...
Autores principales: | Ye, Liu, Gu, Qiang-Shuai, Tian, Yu, Meng, Xiang, Chen, Guo-Cong, Liu, Xin-Yuan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768789/ https://www.ncbi.nlm.nih.gov/pubmed/29335407 http://dx.doi.org/10.1038/s41467-017-02231-7 |
Ejemplares similares
-
Borylated Cyclopropanes
as Spring-Loaded Entities:
Access to Vicinal Tertiary and Quaternary Carbon Stereocenters in
Acyclic Systems
por: Augustin, André U., et al.
Publicado: (2022) -
Stereodivergent synthesis of vicinal quaternary-quaternary stereocenters and bioactive hyperolactones
por: Zheng, Haifeng, et al.
Publicado: (2018) -
Catalytic enantioselective construction of vicinal quaternary carbon stereocenters
por: Zhou, Feng, et al.
Publicado: (2020) -
Asymmetric intramolecular α-cyclopropanation of aldehydes using a donor/acceptor carbene mimetic
por: Luo, Chaosheng, et al.
Publicado: (2015) -
Synthesis of bicyclo[3.1.0]hexanes by (3 + 2) annulation of cyclopropenes with aminocyclopropanes
por: Muriel, Bastian, et al.
Publicado: (2019)