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Chemical ionization mass spectrometry of bifunctional cyclopentanes and cyclohexanes. A correlation between stereochemistry and chemical ionization spectra
24
Citations
29
References
1977
Year
Chemical Ionization SpectraBiological Mass SpectrometryOrganic ChemistryChemistryChemical DerivativeGas ChromatographyAnalytical ChemistryStereoselective SynthesisChemical MeasurementBiochemistryYield Quasimolecular IonsBifunctional CyclopentanesTrans IsomersPharmacologyAcetic Acid EstersHeterocyclicNatural SciencesMass SpectrometryMedicineDrug Analysis
Abstract A correlation has been fround between the stereochemistry of 3‐methoxyeyclopentyl and 3‐methoxyccyelohexyl acetic acid esters and their methane or isobutane themical ionizaion spectra: only the cis compounds yield quasimolecular ions and the [MHCH 3 OH] + ions are more abundant for the trans isomers. A similar situation occurs in the iow temperature methane chemical ionization spectra of the coresponding trimethylsilylethers.
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