| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1412064 | Journal of Molecular Structure | 2006 | 4 Pages |
Abstract
The absolute configuration of three contiguous newly generated stereocenters in (1R,2R,3S,5S,1′R)-3-(1′-(4-methoxyphenyl)ethyl)-6,6-dimethylbicyclo [3.1.1] heptan-2-ol (6), stereoselectively prepared from β-pinene in four steps, was established on the basis of 1H NMR data and molecular modeling.
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Organic Chemistry
Authors
Kátia S.P. Perry, Jorge L.O. Domingos, Ayres G. Dias, Sergio Pinheiro, Antonio J.R. da Silva, Paulo R.R. Costa,