Cannabidiol as the Substrate in Acid-Catalyzed Intramolecular Cyclization

[Image: see text] The chemical reactivity of cannabidiol is based on its ability to undergo intramolecular cyclization driven by the addition of a phenolic group to one of its two double bonds. The main products of this cyclization are Δ(9)-THC (trans-Δ-9-tetrahydrocannabinol) and Δ(8)-THC (trans-Δ-...

Descripción completa

Detalles Bibliográficos
Autores principales: Marzullo, Paola, Foschi, Francesca, Coppini, Davide Andrea, Fanchini, Fabiola, Magnani, Lucia, Rusconi, Selina, Luzzani, Marcello, Passarella, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011986/
https://www.ncbi.nlm.nih.gov/pubmed/32991167
http://dx.doi.org/10.1021/acs.jnatprod.0c00436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011986/
https://www.ncbi.nlm.nih.gov/pubmed/32991167
http://dx.doi.org/10.1021/acs.jnatprod.0c00436

Ejemplares similares