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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-...

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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

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