- Protecting group free enantiospecific total syntheses of structurally diverse natural products of the tetrahydrocannabinoid family
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A simple, highly diastereoselective, Lewis acid catalyzed Friedel-Crafts coupling of a cyclic allylic alcohol with resorcinol derivatives has been developed. The method was applied for the enantiospecific total syntheses of structurally diverse natural products such as machaeriol-D, Δ8-THC, Δ9-THC, epi-perrottetinene and their analogues. Synthesis of both natural products and their enantiomers has been achieved with high atom economy, in a protecting group free manner and in less than 6 steps, the longest linear sequence, in a very good overall yield starting from R-(+) and S-(-)-limonene.
- Dethe, Dattatraya H.,Erande, Rohan D.,Mahapatra, Samarpita,Das, Saikat,Kumar B., Vijay
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- CATALYTIC CANNABINOID PROCESSES AND PRECURSORS
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The present disclosure relates to new cannabinoid sulfonate esters and processes for their use to prepare cannabinoids. The disclosure also relates to the use of catalysts and catalytic processes for the preparation of cannabinoids from the cannabinoid sulfonate esters.
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Page/Page column 28; 39; 42-43
(2020/12/07)
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- Synthesis of Bibenzyl Cannabinoids, Hybrids of Two Biogenetic Series Found in Cannabis sativa
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Syntheses of a series of compounds which merge a m-dihydroxybibenzyl with a terpenoid structure, giving a series of hybrid cannabinoids in which products of two major biogenetic routes of Cannabis are united, are described.The compounds made are the biben
- Crombie, Leslie W.,Crombie, W. Mary L.,Firth, David F.
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p. 1263 - 1270
(2007/10/02)
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