Browsing by Author "Bolinger, Andrew Arch 1989-"
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Item 1,3-Dipolar and 1,3,6-Tripolar Reactivity of 3-hydroxy- and 3-amino-1-N-arylazopropenes for Heterocycle Formation(2019-12) Bolinger, Andrew Arch 1989-; May, Jeremy A.; Coltart, Don M.; Teets, Thomas S.; Do, Loi H.; Gilbertson, Scott R.; Cirino, Patrick C.3-Alkoxy-1-N-aryl azopropene structural motifs in the Eschenmoser-Tanabe Fragmentation pathway have been known for almost 50 years, yet one unexploited feature of these intermediates is their putative 1,3-dipole. Described here is a transformation leveraging this reactivity to synthesize an important class of oxygen heterocycles, β,γ-fused bicyclic γ-lactones, by the simple combination of an ester or acyl pyrrole, an α-epoxy-2-nitrophenyl hydrazone, and a base. The products of this reaction, including those containing quaternary centers, are generated with high (up to >25:1) diastereoselectivity. Conveniently, both syn- and anti-fused bicyclic systems can be generated stereoselectively by simply changing the counter-ion of the base, LiHMDS and KHMDS, respectively. This dissertation also describes the development of a new functional group, 3-amino-1-azopropene, and its use in novel annulation strategies leading to N-heterocycles, which are important structures found in drugs and biologically active natural products. The 3-amino-1-azopropene functional group possesses multiple nucleophilic sites and, as such, is expected to inspire the development of a wide range of new synthetic methods and/or find applications in the development of new drugs and materials. Lastly, as part of the continuing effects to develop new reactions for the formation of saturated heterocycles, the conjugated π systems of azoalkenes in 3-hydroxy-azopropenes and 3-amino-1-azopropene were utilized in a [4+2] cyclization reaction in order to achieve ring closure. Compounds were prepared in high (up to >25:1) diastereoselectivity from a cascading Tsuji-Trost [4+2] cycloaddition, producing a wide array of fused tetrahydrofuran- and pyrrolidine- tetrahydropyridazine derivatives.