Cargando…
Efficient syntheses of (–)-crinine and (–)-aspidospermidine, and the formal synthesis of (–)-minfiensine by enantioselective intramolecular dearomative cyclization
Polycyclic alkaloids bearing all-carbon quaternary centers possess a diversity of biological activities and are challenging targets in natural product synthesis. The development of a general and asymmetric catalytic method applicable to the efficient syntheses of a series of complex polycyclic alkal...
Autores principales: | Du, Kang, Yang, He, Guo, Pan, Feng, Liang, Xu, Guangqing, Zhou, Qinghai, Chung, Lung Wa, Tang, Wenjun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628388/ https://www.ncbi.nlm.nih.gov/pubmed/28989658 http://dx.doi.org/10.1039/c7sc01859b |
Ejemplares similares
-
Cobalt-catalyzed enantioselective intramolecular reductive cyclization via electrochemistry
por: Gao, Shiquan, et al.
Publicado: (2023) -
Metal-Free Diastereo- and Enantioselective Dearomative
Formal [3 + 2] Cycloaddition of 2-Nitrobenzofurans and Isocyanoacetate
Esters
por: Laviós, Adrian, et al.
Publicado: (2022) -
Bioinspired enantioselective synthesis of crinine-type alkaloids via iridium-catalyzed asymmetric hydrogenation of enones
por: Zuo, Xiao-Dong, et al.
Publicado: (2017) -
Redox-triggered cascade dearomative cyclizations enabled by hexafluoroisopropanol
por: Li, Shuai-Shuai, et al.
Publicado: (2018) -
Enantioselective synthesis of cyclopenta[b]benzofurans via an organocatalytic intramolecular double cyclization
por: Paz, Bruno Matos, et al.
Publicado: (2017)