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Synthesis Of Functionalized Tetrahydropyridine Derivatives Via Sncl4-Promoted [4+2] Cycloaddition Of Donor-Acceptor Cyclobutanes And Nitriles, David Tong
Electronic Thesis and Dissertation Repository
The formation of carbon-heteroatom bonds is pivotal in obtaining structural frameworks present in a variety of important natural products and bioactive molecules. In that regard, Lewis-acid promoted cycloadditions of strained carbocycles have proven to be powerful tools for the construction of heterocyclic frameworks. The Pagenkopf group was the first to discover the cycloaddition of donor-acceptor (DA) cyclopropanes with nitriles. Since the strain energy of cyclobutane is comparable to that of cyclopropane, our group has sought to extend to the comparatively unexplored homologous cyclobutane scaffold. Disclosed here is the first [4+2] cycloaddition of nitriles with DA cyclobutanes via Lewis-acid activation. This …
Synthesis Of Functionalized Tetrahydropyridines By Sncl4-Mediated [4+2] Cycloaddition Between Donor–Acceptor Cyclobutanes And Nitriles, David Tong, Jackie Wu, Nathan Bazinski, Donghyun Koo, Naresh Vemula, Brian Pagenkopf
Synthesis Of Functionalized Tetrahydropyridines By Sncl4-Mediated [4+2] Cycloaddition Between Donor–Acceptor Cyclobutanes And Nitriles, David Tong, Jackie Wu, Nathan Bazinski, Donghyun Koo, Naresh Vemula, Brian Pagenkopf
Chemistry Publications
Cycloadditions of strained carbocycles promoted by Lewis acids are powerful methods to construct heterocyclic frameworks. In fact, the formal [3+2] cycloadditions of donor-acceptor (DA) cyclopropanes with nitriles has seen particular success in synthesis. In this work, we report on the first [4+2] cycloaddition of nitriles with DA cyclobutanes via Lewis acid activation. Tetrahydropyridine derivatives were obtained in up to 91% yield from various aryl activated cyclobutane diesters and aliphatic or aromatic nitriles.