Eremophila clarkei

Cembranoids The first macrocyclic diterpene isolated from an Eremophila species was the triol (99) produced by E. clarkei (96). The resin obtained from this plant was a complex mixture of compounds from which the crystalline triol could be obtained with difficulty from the neutral fraction. Larger quantities of triol were available after methylation and lithium aluminium hydride reduction of the acidic fraction. The plane structure of 99 was established by conversion of the triol to a crystalline stereoisomer of cembrane (100) as shown in Scheme 25. The two dihydrotriols (101 and 102) obtained in this sequence also served to prove the location of the hydioxymethylene groups on the cembrane skeleton. Since both 101 and 102 are optically active, the symmetrical 4,12-cis arrangement of the primary alcohol groups can be excluded. Furthermore, the 4, 2-trans-disposition of these groups can also be excluded since elimination of the asymmetry at Cl leads to two different olefins (103 and 104). 

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See also in sourсe #XX -- [ , ]

See also in sourсe #XX -- [ , ]

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