Author:
Ridley DD,Ritchie E,Taylor WC
Abstract
Attempts to separate the
major constituents of the phenolic fraction of the ether extract of the wood of
Grevillea striata R.Br.
were unsuccessful, but by chemical degradation and spectroscopic methods the
structures of four of the components were deduced. They were mono- and di-methyl ethers of 17,19,22,24- tetrahydroxy(l4-p-0-o)cyclophane
with a double bond at either of two positions in the aliphatic chain. The new
ring system was given the trivial name "turriane".
Evidence that a fifth and a sixth component were derivatives with a saturated
chain, and a seventh was a derivative of a double homologue of turriane, was obtained. Synthetic experiments connected
with the structure determination, and on the synthesis of tetrahydroxyturriane
are described. Possible biogenetic routes to striatol
and the cyclophanes are discussed.
Cited by
44 articles.
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