
doi: 10.1071/ch05144
Data concerning the 3-hydroxycineoles 1 and 2 are provided to enable the ready identification of these metabolites and to determine their enantiomeric excess in mixtures. An unusual SN2-type inversion at a tertiary center is observed during one synthetic approach.
780103 Chemical sciences, Eucalyptus, Multidisciplinary, Oxygenated Derivatives, Monoterpene, Alpinia-galanga Willd, Chemistry, C1, Oxidation, Metabolites, Constituents, 1,3,3-trimethyl-2-oxabicyclo<2.2.2>octane 1,8-cineole, 250301 Organic Chemical Synthesis, Biotransformation
780103 Chemical sciences, Eucalyptus, Multidisciplinary, Oxygenated Derivatives, Monoterpene, Alpinia-galanga Willd, Chemistry, C1, Oxidation, Metabolites, Constituents, 1,3,3-trimethyl-2-oxabicyclo<2.2.2>octane 1,8-cineole, 250301 Organic Chemical Synthesis, Biotransformation
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 12 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
