Cargando…
Highly enantioselective access to cannabinoid-type tricyles by organocatalytic Diels–Alder reactions
After prosperous domino reactions towards benzopyrans, the products were used as the starting material in Lewis acid catalyzed and organocatalytic Diels–Alder reactions to build up a tricyclic system. Herein, an asymmetric induction up to 96% enantiomeric excess was obtained by the use of imidazolid...
Autores principales: | Bräse, Stefan, Volz, Nicole, Gläser, Franziska, Nieger, Martin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458765/ https://www.ncbi.nlm.nih.gov/pubmed/23019475 http://dx.doi.org/10.3762/bjoc.8.160 |
Ejemplares similares
-
The Diels‐Alder Approach towards Cannabinoid Derivatives and Formal Synthesis of Tetrahydrocannabinol (THC)
por: Hurrle, Thomas, et al.
Publicado: (2021) -
Organocatalytic Strategies for the Development of the Enantioselective Inverse‐electron‐demand Hetero‐Diels‐Alder Reaction
por: Laina‐Martín, Víctor, et al.
Publicado: (2021) -
Enantioselective Organocatalytic Diels–Alder Trapping of Photochemically Generated Hydroxy‐o‐Quinodimethanes
por: Dell'Amico, Luca, et al.
Publicado: (2016) -
Enantioselective Diels–Alder reaction of anthracene by chiral tritylium catalysis
por: Zhang, Qichao, et al.
Publicado: (2019) -
Chiral‐at‐Iron Catalyst for Highly Enantioselective and Diastereoselective Hetero‐Diels‐Alder Reaction
por: Hong, Yubiao, et al.
Publicado: (2021)