Regioselective C-2 and C-6 Substitution of (S)-Nicotine and Nicotine Derivatives

Abstract
Regioselective deprotonations of (S)-nicotine and derivatives at the C-2 and C-6 positions of the pyridine ring were performed in good to excellent yields. These methodologies allow the direct introduction of a plethora of functional groups onto the pyridine ring of nicotine.

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