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The ISO ‐Tetrahydrocannabinols
Author(s) -
Gaoni Y.,
Mechoulam R.
Publication year - 1968
Publication title -
israel journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.908
H-Index - 54
eISSN - 1869-5868
pISSN - 0021-2148
DOI - 10.1002/ijch.196800086
Subject(s) - chemistry , moiety , terpene , ring (chemistry) , cannabinoid , molecule , stereochemistry , group (periodic table) , organic chemistry , combinatorial chemistry , biochemistry , receptor
Synthetic routes are described which lead to iso‐tetrahydrocannabinols, a new series of structural isomers of the natural Δ 1 ‐tetrahydrocannabinol. In this group of compounds a dihydrobenzopyran ring system is formed by cyclization of one of the phenolic groups of a cannabinoid with the C 1 carbon in the terpene moiety of the molecule.
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