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- W2071356717 abstract "N-(3-Pyridyl)-pyrrole is converted at 710-720°into a mixture of 2-(3-pyridyl)-pyrrole, m.p. 100.8°and 3- (3-pyridyl)-pyrrole, m.p. 137.5°. β-Nicotyrine was prepared from the pyridylpyrrole melting at 100.8°, in consequence of which the structure of this compound is settled. This same pyridylpyrrole is identical with the compound obtained by Ehrenstein by the dehydrogenation of nornicotine and by Späth by the dehydrogenation of myosmine and l-nornicotine. The C-(3-pyridyl)-pyrrole, m.p. 72°, which formed the starting material for the synthesis of nicotine by Pictet was not a pure substance but probably a mixture of both isomeric C-(3-pyridyl)-pyrroles." @default.
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- W2071356717 date "2010-09-03" @default.
- W2071356717 modified "2023-10-14" @default.
- W2071356717 title "Formation of 2-(3-pyridyl)-pyrrole and 3-(3-pyridyl)-pyrrole by the thermal decomposition of n-(3-pyridyl)-pyrrole" @default.
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- W2071356717 doi "https://doi.org/10.1002/recl.19380570715" @default.
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