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- W1970083056 abstract "Several methods have been worked out to synthesize 1 - vinyl - 4 - substituted - Δ2 - tetrazolin - 5 - ones. NMR spectra showed typical AMX-patterns for the vinyl protons with chemical shifts and coupling constants almost independent of the nature of the other N-substituent. From the shielding increments, it was concluded that the tetrazolinone group exercises a strong inductive electron-withdrawing effect, but only a small resonance effect on the vinyl group. This paper also describes the first cycloreversions of azide adducts, induced by electron impact. Other significant fragmentation patterns of several mono- and disubstituted tetrazolinones are discussed." @default.
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- W1970083056 date "1975-01-01" @default.
- W1970083056 modified "2023-10-14" @default.
- W1970083056 title "Synthesis and spectral characteristics of vinyltetrazolinones" @default.
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- W1970083056 doi "https://doi.org/10.1016/0040-4020(75)80081-0" @default.
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