1961
DOI: 10.1002/9780470186657.ch3
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Alkylpyridines and Arylpyridines

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Cited by 3 publications
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“…Of the three isomers, 3-methylpyridine is the least reactive [18], but under pyrolysis conditions the decomposition reactivity is reversed, with 3-methylpyridine being the most reactive for decomposition at around 800 °C [19]. From Table 3, the relative NPD responses were in the order: 3-methylpyridine (1) > 4-methylpyridine (0.95) > 2-methylpyridine (0.69).…”
Section: Impact Of Molecular Structure Of Isomers On Cyano-radical Fomentioning
confidence: 98%
“…Of the three isomers, 3-methylpyridine is the least reactive [18], but under pyrolysis conditions the decomposition reactivity is reversed, with 3-methylpyridine being the most reactive for decomposition at around 800 °C [19]. From Table 3, the relative NPD responses were in the order: 3-methylpyridine (1) > 4-methylpyridine (0.95) > 2-methylpyridine (0.69).…”
Section: Impact Of Molecular Structure Of Isomers On Cyano-radical Fomentioning
confidence: 98%