2017
DOI: 10.1007/s11172-017-1761-4
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Ambiguousness of GC-MS identification of spiro[2.4]hepta-4,6-diene in natural objects

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Cited by 5 publications
(2 citation statements)
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“…This is caused by objectively higher information content of the mass spectra compared with one‐dimensional chromatographic data . Nevertheless, just chromatographic data appeared to be useful in identification of analytes with undistinguishable mass spectra, namely, isomers (see examples in the Introduction). Thus, the search for approaches of really joint interpretation of MS and GC data seems highly desirable.…”
Section: Resultsmentioning
confidence: 99%
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“…This is caused by objectively higher information content of the mass spectra compared with one‐dimensional chromatographic data . Nevertheless, just chromatographic data appeared to be useful in identification of analytes with undistinguishable mass spectra, namely, isomers (see examples in the Introduction). Thus, the search for approaches of really joint interpretation of MS and GC data seems highly desirable.…”
Section: Resultsmentioning
confidence: 99%
“…However, the verification of these results using GC RIs indicates that these data belong to four different hydrocarbons with similar mass spectra . Another paradox is the identification of a rather “exotic” bicyclic hydrocarbon, spiro[2.4]hepta‐4,6‐diene, which was reported more than ten times in different natural objects during 2010–2016 . The reason for errors in this case is the similarity of the mass spectra of this compound (C 7 H 8 ) and such isomeric petroleum hydrocarbons as toluene…”
Section: Introductionmentioning
confidence: 97%