Cargando…
Chiral phosphoric acid catalyzed aminative dearomatization of α-naphthols/Michael addition sequence
Asymmetric dearomatization reactions have recently emerged as a powerful tool for the rapid build-up of the molecular complexity. Chiral three-dimensional polycyclic molecules bearing contiguous stereogenic centers can be synthesized from readily available planar aromatic feedstocks. Here we report...
Autores principales: | Xia, Zi-Lei, Zheng, Chao, Xu, Ren-Qi, You, Shu-Li |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637135/ https://www.ncbi.nlm.nih.gov/pubmed/31316064 http://dx.doi.org/10.1038/s41467-019-11109-9 |
Ejemplares similares
-
Construction of spirocarbocycles via gold-catalyzed intramolecular dearomatization of naphthols
por: Wu, Wen-Ting, et al.
Publicado: (2016) -
Organocatalytic asymmetric chlorinative dearomatization of naphthols
por: Yin, Qin, et al.
Publicado: (2015) -
Lewis Acid Promoted Dearomatization of Naphthols
por: Kulish, Kirill, et al.
Publicado: (2020) -
Catalytic asymmetric hydroxylative dearomatization of 2-naphthols: synthesis of lacinilene derivatives
por: Zhang, Yu, et al.
Publicado: (2017) -
Asymmetric addition of α-branched cyclic ketones to allenamides catalyzed by a chiral phosphoric acid
por: Yang, Xiaoyu, et al.
Publicado: (2016)