Polyacetylene alcohols structure

From the ether-soluble fraction, Takahashi etal. 134, 135) isolated sitosterol-P-D-glucoside, sitosterol, p-elemene (96), eremophilene (97) and a new polyacetylenic alcohol named panaxynol (98), the structure of which was elucidated as heptadeca-l,9(Z)-diene-4,6-diyn-3-ol by degradative and synthetic procedures. It is identical with carotatoxin from carrots 136) and falcarinol from Falcaria vulgaris 137). Recently two other polyacetylenic alcohols, 9,10-epoxy-3-hydroxyheptadeca-l-en-4,6-diyne [(99), panaxydol] 138) and heptadeca-l-en-4,6-diyn-3,9-diol (100) 139) were isolated from Ginseng roots by Wrobel et al. 

Among the classical (summarized in [11]) reactions of cyanoacetylenes (salt and n-complex formation, nucleophilic addition of, inter alia, amines and alcohols, Diels-Alder additions with 2 (see Section 2.22.2), addition of halogens and hydrogen halides, etc.) their polymerization might deserve a second look since the products formed - polyacetylenes - have attracted much attention during the last two decades. Thus 1, several of its derivatives, and 2 have been polymerized with anionic initiators (triethylamine, sodiiun cyanide, butyllithium) to give black, low-molecular-weight polymers claimed to have structures like 33 [38-40], which is obtained from 2 by treatment with butyllithium. 

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