Cannabidiol as the Substrate in Acid-Catalyzed Intramolecular Cyclization.
Journal
Journal of natural products
ISSN: 1520-6025
Titre abrégé: J Nat Prod
Pays: United States
ID NLM: 7906882
Informations de publication
Date de publication:
23 10 2020
23 10 2020
Historique:
pubmed:
30
9
2020
medline:
21
9
2021
entrez:
29
9
2020
Statut:
ppublish
Résumé
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
Identifiants
pubmed: 32991167
doi: 10.1021/acs.jnatprod.0c00436
pmc: PMC8011986
doi:
Substances chimiques
Cannabinoids
0
Cannabidiol
19GBJ60SN5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2894-2901Références
Acta Pharmacol Sin. 2019 Mar;40(3):300-308
pubmed: 29941868
Nat Prod Rep. 2016 Nov 23;33(12):1357-1392
pubmed: 27722705
Trends Pharmacol Sci. 2009 Oct;30(10):515-27
pubmed: 19729208
AAPS J. 2004 Oct 19;6(4):e30
pubmed: 15760095
Sci Justice. 2018 Sep;58(5):355-365
pubmed: 30193661
Adicciones. 2018 Apr 15;30(2):140-151
pubmed: 28492950
J AOAC Int. 2015 Nov-Dec;98(6):1523-8
pubmed: 26651563
Phytochem Anal. 2004 Nov-Dec;15(6):345-54
pubmed: 15595449
Chem Phys Lipids. 2002 Dec 31;121(1-2):35-43
pubmed: 12505688
J Am Chem Soc. 1971 Jan 13;93(1):217-24
pubmed: 5538858
Neurotherapeutics. 2015 Oct;12(4):699-730
pubmed: 26264914
Br J Pharmacol. 2008 Jan;153(2):199-215
pubmed: 17828291