Semiochemicals via epoxide inversion
Copyright policy ) J E, Oliver; R M, Waters; D J, Harrison;
Semiochemicals via epoxide inversion
A sequence of reactions is presented for inverting the configurations of both epoxide carbons in 1,2-disubstituted epoxides. As examples, (+)-disparlure was converted to its enantiomer, (-)-disparlure, andexo-endo conversion of a cyclohexene oxide was demonstrated.
- Agricultural Research Service United States
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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).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 4
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