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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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| Gepubliceerd in: | J Nat Prod |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Chemical
Society and American
Society of Pharmacognosy
2020
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| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8011986/ https://ncbi.nlm.nih.gov/pubmed/32991167 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.jnatprod.0c00436 |
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