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| | Isomerization of the unsaturated alcohols (Site not responding. Last check: ) |
 | | The unsaturated alcohols represented by the general formulas (I) and (II) may also be used as a reagent to prepare the catalyst. |
 | | Examples of the unsaturated alcohols by the general formula (I) are 2-methyl-3-butene-2-ol, linalool (3,7-dimethyl-1,6-octadiene-3-ol), 3,7-dimethyl-1-octene-3-ol, 3-ethyl-7-methyl-1,6-octadiene-3-ol, 3,7-dimethyl-7-ethoxy-1-octene-3-ol, 2-benzyl-3-butene-2 -ol, nerolidol (3,7,11-trimethyl-1,6,10-dodecatriene-3-ol), isophytol (3,7,11,15-tetramethyl-1-nexadecene-3-ol), 3,7,11,15-tetramethyl-1,6,10,14-hexadecatetraene-3-ol, 1-vinyl cyclohexanol, cyclonerolidol ((5-(2,6,6-trimethyl-1-cyclohexenyl)-3-methyl-1-pentene-3-ol)), 1-hexene-3-ol, 3,7-dimethyl-1-octene-3,7-diol, 9-(2,6,6-trimethyl-1-cyclohexenyl)-3,7-dimethyl-1,4,6,8-nonatetraene-3-ol, and 2,3-dimethyl-3-butene-2-ol. |
 | | The process of the invention may be applicable to produce the unsaturated alcohols represented by the general formula (II) from those of the general formula (I) in the same manner as illustrated to produce geraniol or nerol from linalool. |
| www.sacnewsmonthly.com /invent/process_modifying_capillary_grooves/isomerization_unsaturated_alcohols.html (4650 words) |
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