Cannabidiol as the Substrate in Acid-Catalyzed Intramolecular Cyclization.

ABSTRACT: 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 Δ⁹-THC (trans-Δ-9-tetrahydrocannabinol) and Δ⁸-THC (trans-Δ-8-tetrahydrocannabinol). These two cannabinoids are isomers, and the first one is a frequently investigated psychoactive compound and pharmaceutical agent. The isomers Δ⁸-iso-THC (trans-Δ-8-iso-tetrahydrocannabinol) and Δ⁴⁽⁸⁾-iso-THC (trans-Δ-4,8-iso-tetrahydrocannabinol) have been identified as additional products of intramolecular cyclization. The use of Lewis and protic acids in different solvents has been studied t

SUBMITTER: Marzullo P 

PROVIDER: S-EPMC8011986 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature