Cargando…
Natural Product Synthesis Enabled by Domino Processes Incorporating a 1,2-Rearrangement Step
[Image: see text] The art of natural product total synthesis is closely associated with two major determinants: the development/application of novel chemical reactions and the innovation in strategic use of classic organic reactions. While purposely seeking/applying a new synthetic methodology allow...
Autores principales: | Delayre, Bastien, Wang, Qian, Zhu, Jieping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155462/ https://www.ncbi.nlm.nih.gov/pubmed/34056086 http://dx.doi.org/10.1021/acscentsci.1c00075 |
Ejemplares similares
-
Four‐Step Domino Reaction Enables Fully Controlled Non‐Statistical Synthesis of Hexaarylbenzene with Six Different Aryl Groups
por: Grau, Benedikt W., et al.
Publicado: (2021) -
C–C bond activation enabled by dyotropic rearrangement of Pd(IV) species
por: Cao, Jian, et al.
Publicado: (2021) -
Multicomponent Domino Reaction in the Asymmetric Synthesis of Cyclopentan[c]pyran Core of Iridoid Natural Products
por: Manchado, Alejandro, et al.
Publicado: (2020) -
An Efficient Synthesis of Acenaphtho[1,2-b]indole Derivatives via Domino Reaction
por: Zhang, Guo-Ning, et al.
Publicado: (2018) -
Dual-Metal Single
Atoms with Dual Coordination for
the Domino Synthesis of Natural Flavones
por: Zhao, Xin, et al.
Publicado: (2023)