SYNTHESIS OF THE INDIVIDUAL, PHARMACOLOGICALLY DISTINCT, ENANTIOMERS OF A TETRAHYDROCANNABINOL DERIVATIVE

DOI: 10.1016/S0957-4166(00)86322-3

Source and publish data:

Tetrahedron Asymmetry p. 315 - 318 (1990)

Update date:2022-07-30

Topics:

Authors:

Mechoulam, Raphael

Lander, Naftali

Breuer, Aviva

Zahalka, Jamal

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Article abstract of DOI:10.1016/S0957-4166(00)86322-3

The individual enantiomers of the 1,1-dimethylheptyl homolog of 7-hydroxy-Δ⁶-tetrahydrocannabinol, (1) and (2a), which exhibit distinct pharmacological profiles, have been obtained with very high e.e. by synthesis from the antipodes of myrtenol.

Full text of DOI:10.1016/S0957-4166(00)86322-3

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