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Complete 1 H and 13 C NMR Spectral Assignment of δ‐Cadinene, a Bicyclic Sesquiterpene Hydrocarbon
Author(s) -
Davis G. D.,
Essenberg M.,
Berlin K. D.,
Faure R.,
Gaydou E. M.
Publication year - 1996
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/(sici)1097-458x(199602)34:2<156::aid-omr859>3.0.co;2-2
Subject(s) - chemistry , hydrocarbon , bicyclic molecule , sesquiterpene , nuclear magnetic resonance spectroscopy , carbon 13 nmr , stereochemistry , analytical chemistry (journal) , organic chemistry
δ‐Cadinene from cade oil and ylang‐ylang essential oil was independently analyzed by two research groups employing 2D NMR spectroscopy to effect the complete assignment of 1 H and 13 C spectra and to confirm the previously reported structure of δ‐cadinene.