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A new look at the spectroscopic properties of dihydrocarveol stereoisomers

 

作者: M. Decouzon,   S. Géribaldi,   M. Rouillard,   J.‐M. Sturla,  

 

期刊: Flavour and Fragrance Journal  (WILEY Available online 1990)
卷期: Volume 5, issue 3  

页码: 147-152

 

ISSN:0882-5734

 

年代: 1990

 

DOI:10.1002/ffj.2730050303

 

出版商: John Wiley&Sons, Ltd.

 

关键词: Dihydrocarveol;Fourier transform mass spectrometry (FT‐MS);Fourier transform ion cyclotron resonance (FT‐ICR);Negative ion chemical ionization (NICI);Collision‐induced dissociation (CID);Gas Chromatography‐Fourier transform infrared (GC‐FTIR);Fourier tran

 

数据来源: WILEY

 

摘要:

AbstractThe principal spectroscopic properties of the four dihydrocarveol diastereoisomers are reinvestigated. The interpretation of their1H‐NMR spectra allows unambiguous differentiation of the diastereoisomers and the determination of their conformations. ‘Negative ion chemical ionization‐Collision‐induced dissociation’ experiments have been performed on the quasimolecular ions [M ‐ H]−using a FT‐ICR spectrometer. The daughter ion spectra of the alkoxide negative ions [M ‐ H]−of the four isomers show substantial differences which can be used for a diastereoisomeric differentiation and the confirmation of the conformations. The gas phase FT‐IR spectra are recorded. The MS and IR results can be used for essential oil analysis using GC–MS an

 

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