Part I: Asymmetric Synthesis Of α-Allyl-α-Aryl α-Amino Acids Part Ii: Asymmetric Spirocyclization Of Allenyl Ketones Part Iii: Chemoselective Activation Of C(sp3)−h Bond Over C(sp2)−h Bond With Pd(ii)

by John M. Curto

Institution: University of Pennsylvania
Year: 2014
Keywords: Amino Acids; Asymmetric Catalysis; C-H Activation; High-throughput Experimentation; Methodology and Reactions; Reaction Mechanisms; Organic Chemistry
Record ID: 2026461
Full text PDF: http://repository.upenn.edu/edissertations/1063



Part I. The first asymmetric synthesis of a-allyl-a-aryl a-amino acids by means of a three component coupling of a-iminoesters, Grignard reagents, and cinnamyl acetate is reported. Notably, the enolate from the tandem process provides a much higher level of reactivity and selectivity than the same enolate generated via direct deprotonation, presumably due to differences in the solvation/aggregation state. A novel method for removal of a homoallylic amine protecting group delivers the free amine congeners. The a-allyl moiety offers a means to generate further valuable a-amino acid structures. Cross-metathesis of the tandem product provided allylic diversity not afforded in the parent reaction. Cyclic a-amino acid derivatives could be accessed by ring closing metathesis presenting a viable strategy to higher ring homologues of enantioenriched a-substituted proline. The 8-member proline analog was successfully converted to the pyrrolizidine natural product backbone. Part II. The asymmetric spirocyclization of allenyl ketones is reported. High-throughput experimentation by means of a chiral Lewis acid library enabled the determination of a suitable catalyst system. Protecting group manipulation provides an orthogonal route to enantioenriched para-quinone and ortho-quinone spirocycles. This novel technology provides access to the spirocyclic core that is prevalent in many natural products. Part III. Palladium has been identified as a suitable catalyst for the chemoselective activation of C(sp3)-H bond over C(sp2)-H bond of toluene and tolyl analogs. This technology has been combined with the C(sp3)-H activation of acidic C-H bonds to form new C-C bonds. High-throughput experimentation was used for identifying conditions that reduced toluene loading and engendered catalyst turnover via a suitable oxidant. The parent reaction has been extended to include the Pd catalyzed alkylation of phenylglycine azlactones with ethylbenzene, 2-ethylnaphthalene, propylbenzene and butylbenzene. Mechanistic studies were initiated to determine whether the process occurs via free radicals or via Pd mediated C(sp3)-H activation. Our studies support a Pd mediated process in which the C(sp3)-H activation of the tolyl analog is the rate determining step. This finding represents a paradigm shift in our understanding of Pd and its selectivity for arene activation vs benzylic activation.