Cargando…
Successive Diels–Alder Cycloadditions of Cyclopentadiene to [10]CPP⊃C(60): A Computational Study
[Image: see text] Fullerenes have potential applications in many fields. To reach their full potential, fullerenes have to be functionalized. One of the most common reactions used to functionalize fullerenes is the Diels–Alder cycloaddition. In this case, it is important to control the regioselectiv...
Autores principales: | Pareras, Gerard, Simon, Sílvia, Poater, Albert, Solà, Miquel |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016765/ https://www.ncbi.nlm.nih.gov/pubmed/35319187 http://dx.doi.org/10.1021/acs.joc.1c03116 |
Ejemplares similares
-
On the regioselectivity of the Diels–Alder cycloaddition to C(60) in high spin states
por: El Bakouri, Ouissam, et al.
Publicado: (2018) -
Roles of Lewis Acid Catalysts in Diels‐Alder Reactions between Cyclopentadiene and Methyl Acrylate
por: Sakata, Ken, et al.
Publicado: (2020) -
Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene
por: Rueping, Magnus, et al.
Publicado: (2012) -
Diels–Alder Cycloaddition Reactions in Sustainable Media
por: Soares, Maria I. L., et al.
Publicado: (2022) -
Diels–Alder reactions between cyclopentadiene analogs and benzoquinone in water and their application in the synthesis of polycyclic cage compounds
por: Shi, Yijun, et al.
Publicado: (2020)