Infinitesimal Progress : Rethinking Bergsonian Modalities of Time in William Faulkner\u27s Novels, 1929-1932

William Faulkner’s depictions of the past are as ornate as they are inescapable. His characters cannot escape the perpetual imposition of the past upon the present; entire lineages fall victim to the flaws of their fathers, history is as cyclical as the movements of a wagon along a dusty Mississippi road. This thesis explains the Bergsonian mechanics of duration present in The Sound and the Fury, As I Lay Dying, and Light in August and reevaluates the fatalistic implications Faulkner’s macabre characters face recursively in and through time. Much of the critical exploration of time in Faulkner’s fiction is outmoded and does not correspond with current modes of analysis, particularly race and gender studies. However, a critical reevaluation of Faulkner’s fatalistic depictions of time offers new studies a different undertaking. This thesis explores the implications of reuniting Bergsonism and three of Faulkner’s novels, concentrating on the significant implications wagons and wagon wheels bear on a paradoxically static but perpetually moving time. Through this reading, this thesis offers a nuanced account of what temporal modalities in Faulkner might amount to in this century

H2 molecule in strong magnetic fields

The Pauli-Hamiltonian of a molecule with fixed nuclei in a strong constant magnetic field is asymptotic, in norm-resolvent sense, to an effective Hamiltonian which has the form of a multi-particle Schr\"odinger operator with interactions given by one-dimensional \delta-potentials. We study this effective Hamiltonian in the case of the H2 -molecule and establish existence of the ground state. We also show that the inter-nuclear equilibrium distance tends to 0 as the field-strength tends to infinity

Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids

Enantioselective Pd-catalyzed allylic alkylations of prochiral enolates represent a powerful tool for the construction of all-carbon quaternary stereocenters. This review describes the emergence of such reactions as strategic linchpins that enable efficient, stereocontrolled syntheses of Aspidosperma and related monoterpene indole alkaloids

Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids

Enantioselective Pd-catalyzed allylic alkylations of prochiral enolates represent a powerful tool for the construction of all-carbon quaternary stereocenters. This review describes the emergence of such reactions as strategic linchpins that enable efficient, stereocontrolled syntheses of Aspidosperma and related monoterpene indole alkaloids

The Value of Comparative Animal Research : Krogh’s Principle Facilitates Scientific Discoveries

There are no conflicts of interest to declare. This paper developed from the 2016 Early Career Impact Award from the Federation of Associations in Behavioral & Brain Sciences to TJS. TJS has received funding from The Leverhulme Trust. FJPE is in receipt of funding from the BBSRC (BB/M001555/1). The National Institutes of Health has funded RDF (NS 034950, NS093277, NIMH 087930), AGO (HD079573, IOS-1354760) and AMK (HD081959). BAA is an Arnold O. Beckman postdoctoral fellow.Peer reviewedPostprin

The Total Synthesis of (–)-Scabrolide A

The first total synthesis of the norcembranoid diterpenoid scabrolide A is disclosed. The route begins with the synthesis of two chiral pool-derived fragments, which undergo a convergent coupling to expediently introduce all 19 carbon atoms of the natural product. An intramolecular Diels–Alder reaction and an enone–olefin cycloaddition/fragmentation sequence are then employed to construct the fused [5–6–7] linear carbocyclic core of the molecule and complete the total synthesis

Angular Power Spectrum Estimation of Cosmic Ray Anisotropies with Full or Partial Sky Coverage

We study the angular power spectrum estimate in order to search for large scale anisotropies in the arrival directions distribution of the highest-energy cosmic rays. We show that this estimate can be performed even in the case of partial sky coverage and validated over the full sky under the assumption that the observed fluctuations are statistically spatial stationary. If this hypothesis - which can be tested directly on the data - is not satisfied, it would prove, of course, that the cosmic ray sky is non isotropic but also that the power spectrum is not an appropriate tool to represent its anisotropies, whatever the sky coverage available. We apply the method to simulations of the Pierre Auger Observatory, reconstructing an input power spectrum with the Southern site only and with both Northern and Southern ones. Finally, we show the improvement that a full-sky observatory brings to test an isotropic distribution, and we discuss the sensitivity of the Pierre Auger Observatory to large scale anisotropies.Comment: 16 pages, 6 figures, version accepted for publication by JCA

Enantioselective Catalysis Coupled with Stereodivergent Cyclization Strategies Enables Rapid Syntheses of (+)-Limaspermidine and (+)-Kopsihainanine A

Enantioselective Pd-catalyzed allylic alkylations of dihydropyrido[1,2-a]indolone (DHPI) substrates were used to construct the C20-quaternary stereocenters of multiple monoterpene indole alkaloids. Stereodivergent Pictet–Spengler and Bischler–Napieralski cyclization/reduction cascades furnish the cis- and trans-fused azadecalin subunits present in Aspidosperma and Kopsia alkaloids, respectively, en route to highly efficient syntheses of (+)-limaspermidine and (+)-kopsihainanine A

Enantioselective Pd-Catalyzed Allylic Alkylation Reactions of Dihydropyrido[1,2-a]indolone Substrates: Efficient Syntheses of (−)-Goniomitine, (+)-Aspidospermidine, and (−)-Quebrachamine

The successful application of dihydropyrido[1,2-a]indolone (DHPI) substrates in Pd-catalyzed asymmetric allylic alkylation chemistry facilitates rapid access to multiple alkaloid frameworks in an enantioselective fashion. Strategic bromination at the indole C3 position greatly improved the allylic alkylation chemistry and enabled a highly efficient Negishi cross-coupling downstream. The first catalytic enantioselective total synthesis of (−)-goniomitine, along with divergent formal syntheses of (+)-aspidospermidine and (−)-quebrachamine, are reported herein