## Abstract Two novel cannabinoid model compounds, (3__R__, 4__R__)‐Δ^1(6)^‐tetrahydrocannabinol‐5″‐oic acid **(22)** and 4″(__R__, __S__)‐methyl‐(3__R__, 4__R__)‐Δ^1(6)^‐tetrahydrocannabinol‐5″‐oic acid **(23)** were synthesized by acid‐catalyzed condensation of (+)‐__trans‐p__‐mentha‐2, 8‐dien‐l‐
Microbial transformation of cannabinoids. Part 3: Major metabolites of (3R, 4R)-Δ1-tetrahydrocannabinol
✍ Scribed by Michael Binder; Astrid Popp
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- German
- Weight
- 249 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The metabolic transformations of the psychotropic cannabinoid (3__R__, 4__R__)‐Δ^1^‐tetrahydrocannabinol (5) (=Δ^1^‐THC) by cultures of Fusarium Nivale, Gibberella fujikuroi (both Ascomycetes) and Thamnidium elegans (Phycomycetes) were investigated. A number of metaboilites, 1–4 and 6–9 were isolated from the incubations, partly purified and their structures elucidated by combined gas chromatography/mass spectrometry. Four of these metabolites, 1″‐hydroxy‐Δ^1^‐THC (4) 2″‐hydroxy‐β^1^‐THC (1) 6Δ‐hydroxy‐ζ^1^‐THC (8) and 2″,6Δ‐dihydroxy‐Δ^1^‐THC (9) so far have not been reported as microbial transformation products of 5.
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