In this investigation the addition of hydrogen bromide
to 3-methylcyclohexene has been studied in order to see if
the theory of hyperconjugation could be extended to include
olefins of this type. Since the olefin has an equal number
of hydrogens on both carbons carrying the double bond, a
mixture of...
The possibility of synthesizing 1, 8-naphthyridines by the Doebner reaction has appeared in many reports. The method involves the introduction of electron releasing groups in the 6-position of 2-amino pyridine to activate the C-3 position. Previously Lewis used 6-methyl-2-amino pyridine with benzaldehyde and pyruvic acid, in an attempt to prepare...