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Published on: August 12, 2019
Michael Addition with an Olefinic Pyridine: Organometallic Nucleophiles and Carbon Electrophiles
Michael R Stentzel1, Douglas A Klumpp1
1Department of Chemistry and Biochemistry Northern Illinois University DeKalb, Illinois 60115, United States.
Abstract:
The conjugate addition reactions of trans-1,2-di(2-pyridyl)ethylene have been studied. This substrate reacts with organolithium nucleophiles, and the resulting anionic intermediates may be trapped by proton or various carbonyl-based electrophiles. It is suggested that the dipyridyl structure stabilizes the intermediate carbanion, allowing the Michael adduct to be captured by an added electrophile.
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