2021
DOI: 10.1002/chem.202002887
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Cannabidiol Discovery and Synthesis—a Target‐Oriented Analysis in Drug Production Processes

Abstract: Figure 3. Chemical structure of (À)-2. Scheme3.Natural intermediates in the biosynthesiso f(À)-4. Scheme1.The CBD ((À)-2)i solation protocolestablished by Adams and co-workers.

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Cited by 14 publications
(6 citation statements)
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References 233 publications
(530 reference statements)
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“…After a careful assessment of the enantioselective syntheses of CBD, [15] we considered as particularly noteworthy the one recently reported by Leahy et al [16] and we decided to plan the asymmetric total synthesis of CBD-C 4 (1) based on the same general strategy. The adaptation of the experimental procedures revealed some critical issues that we have specifically overcome for the CBD-C 4 synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…After a careful assessment of the enantioselective syntheses of CBD, [15] we considered as particularly noteworthy the one recently reported by Leahy et al [16] and we decided to plan the asymmetric total synthesis of CBD-C 4 (1) based on the same general strategy. The adaptation of the experimental procedures revealed some critical issues that we have specifically overcome for the CBD-C 4 synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…Cannabidiol (CBD) is one of at least eighty-five naturally occurring phytocannabinoids found in cannabis plants and accounts for around 40-50% of the crude plant extract alongside other significant phytocannabinoids including cannabidivarin (CBDV), cannabigerol (CBG) and Δ 9 -tetrahydrocannabinol (THC). [1][2][3][4] CBD naturally exists in the plant as cannabidiolic acid (CBDA), which is converted to CBD through thermal decarboxylation upon isolation. 5 CBD was discovered and first isolated in 1940 by the groups of both Adams and Todd, 6,7 with relative and absolute stereochemistry determined by subsequent work from Mechoulam and Sikemeier.…”
Section: Introductionmentioning
confidence: 99%
“…To meet the increasing demand for CBD‐infused products on the market, different synthetic routes to cannabidiol have been proposed (including biotechnological approaches) [5] . Many strategies, often not stereoselective, start with the use of olivetol, as reported in previous reviews [4–8] . However, a dedicated review on the stereoselective synthesis of (−)‐cannabidiol that includes modern approaches (e. g. flow chemistry) has not been covered before.…”
Section: Introductionmentioning
confidence: 99%
“…Not surprisingly, the demand for cannabidiol for health and wellness purposes has dramatically increased in the last decade, fuelled by the rising government approvals of CBD for medical applications [4] . To meet the increasing demand for CBD‐infused products on the market, different synthetic routes to cannabidiol have been proposed (including biotechnological approaches) [5] . Many strategies, often not stereoselective, start with the use of olivetol, as reported in previous reviews [4–8] .…”
Section: Introductionmentioning
confidence: 99%