The chemistry of Eremophila spp. VIII. A cembrenetriol from E. clarkei
The isolation of a triol (1) from the title plant is described. Reduction and deoxygenation of (1) leads to the cembrane (12). The position of the primary hydroxyls is fixed by a stereochemical argument and the relationship of the 1-hydroxy-1-methylethyl group and the double bond is established through the pyrrole (14).
Keyword(s):
1983 ◽
Vol 41
◽
pp. 194-195
Keyword(s):
1970 ◽
Vol 28
◽
pp. 156-157
1991 ◽
Vol 49
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pp. 236-237
Keyword(s):
1985 ◽
Vol 49
(4)
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pp. 207-213
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1985 ◽
Vol 49
(8)
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pp. 573-578
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Keyword(s):
1993 ◽
Vol 2
(3)
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pp. 52-55
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