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- W2075816036 abstract "Mass spectral decomposition process involving intramolecular aromatic substitution with the ejection of either the hydrogen or the substituent in the ortho position from the M+· ion is noticed in the eleven 5-(arylmethylene) barbituric acids studied. It has been generally noticed that for such a cyclization to occur, the presence of an α,β-unsaturated carbonyl function, in conjugation with the ring, is essential in aromatic systems." @default.
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- W2075816036 date "1980-10-01" @default.
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- W2075816036 title "Ortho Effects in Organic Molecules on Electron Impact. VIII. Intramolecular Aromatic Substitution in (Arylmethylene)barbituric Acids" @default.
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- W2075816036 doi "https://doi.org/10.1246/bcsj.53.3004" @default.
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