4.7 Article

Synthetic Strategies for Rare Cannabinoids Derived from Cannabis sativa

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 85, Issue 6, Pages 1555-1568

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.2c00155

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Funding

  1. German Federal Ministry of Education and Research [03VP06370]

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Efficient syntheses of eight key cannabinoids have been established and optimized. A variety of reactions were employed to prepare these cannabinoids and their derivatives.
Efficient syntheses of eight key cannabinoids were established and optimized. Predominant cannabinoids such as cannabigerol (CBG-C5) and cannabidiol (CBD-C5) were prepared from olivetol via regioselective condensation. Further treatments of CBD led to Delta 9(CBN-C5). Alternatively, a [3 + 3] annulation between olivetol and citral yielded the minor cannabinoid cannabichromene (CBC-C5), which was converted into two very rare polycycles, cannabicyclol (CBL-C5) and cannabicitran (CBT-C5), in a one-pot reaction. Finally, all eight syntheses were extended by utilizing resorcinol and two phenolic analogues, achieving a cannabinoid group with more than 30 compounds through a facile synthesis strategy.

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