Abstract
The mechanism of formation, and the
chemical and hydrate forming properties of the 1,8-terpins are discussed.
Configurations are assigned to the six 1,8-dihalogeno-p-menthanes,
ethylnopinol, β-terpineol, p-menthan-1-ol, and homoterpin. It is suggested
that the presently accepted configurations of the carveols and sobrerols may
need to be reversed and that the structures of the p-menthane-2,8-diols need
revision.
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7 articles.
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