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Full-Text Articles in Physical Sciences and Mathematics
Enantioselective Biotransformation Of Prochiral Ketone Via Daucus Carota, Ryan Smith, Charlie Knox, Elizabeth Davis
Enantioselective Biotransformation Of Prochiral Ketone Via Daucus Carota, Ryan Smith, Charlie Knox, Elizabeth Davis
Undergraduate Research Conference
Biotransformations of prochiral ketones can be performed using plant cells. The benefits of using plant cells include low cost, environmentally sound procedures compared to conventional chemical processes, and the stereospecific nature of the reaction.1,2 Benzofuran-2-yl methyl ketone was reduced to (- )-benzofuran-2-yl-ethanol after incubation with carrots in water. The reaction was enantioselective in that it produced the S-isomer as indicated by optical activity. Currently, attempts to isolate the carrot enzyme and antimicrobial studies of the (-)-benzofuran-2-yl-ethanol product are underway.
Research In The Teaching Laboratory: Improving The Synthesis Of Lidocaine, Chris Taliaferro
Research In The Teaching Laboratory: Improving The Synthesis Of Lidocaine, Chris Taliaferro
Undergraduate Research Conference
The multi-step synthesis of Lidocaine is traditionally a low-yielding reaction mainly due to its second step, formation of a-chloro-2,6-dimethylacetanilide. Students often question the use of an acid (acetic acid) as the solvent for the reaction of a base (2,6-dimethylaniline, 1) with the acyl chloride (a-chloroacetyl chloride, 2), (Reaction Scheme) but they follow the procedure as directed.
Students, if treated as scientists in training, should be able to form a hypothesis before an experiment, design experiments to test the given hypothesis, and evaluate the results. A typical laboratory class was assigned to synthesize a-chloro-2,6-dimethylacetanilide using …
The Golden Pathway To Thiolate-Stabilized Nanoparticles: Following The Formation Of Gold (I) Thiolate From Gold (Iii) Chloride, Brian M. Barngrover, Christine M. Aikens
The Golden Pathway To Thiolate-Stabilized Nanoparticles: Following The Formation Of Gold (I) Thiolate From Gold (Iii) Chloride, Brian M. Barngrover, Christine M. Aikens
Faculty Publications
Pathways for the formation of gold thiolate complexes from gold(III) chloride precursors AuCl4– and AuCl3 are examined. This work demonstrates that two distinct reaction pathways are possible; which pathway is accessible in a given reaction may depend on factors such as the residue group R on the incoming thiol. Density functional theory calculations using the BP86 functional and a polarized triple-ζ basis set show that the pathway resulting in gold(III) reduction is favored for R = methyl. A two-to-one ratio of thiol or thiolate to gold can reduce Au(III) to Au(I), and a three-to-one ratio can lead …
Toward A Regional Radiocarbon Model For The East Texas Woodland Period, Robert Z. Selden Jr., Timothy K. Perttula
Toward A Regional Radiocarbon Model For The East Texas Woodland Period, Robert Z. Selden Jr., Timothy K. Perttula
CRHR: Archaeology
The East Texas Radiocarbon Database contributes to an analysis of tempo and place for Woodland era (ca. 500 B.C. - A.D. 800) archaeological sites within the region. The temporal and spatial distributions of calibrated radiocarbon (14C) ages (n=127) with a standard deviation (ΔT) of 61 from archaeological sites with Woodland components (n=51) are useful in exploring the development and geographical continuity of the peoples in East Texas, and lead to a refinement of our current chronological understanding of the period. While the analysis of the dates produces less than significant findings due to sample size, they are used …
Modeling Regional Radicarbon Trends: A Case Study From The East Texas Woodland Period, Robert Z. Selden Jr.
Modeling Regional Radicarbon Trends: A Case Study From The East Texas Woodland Period, Robert Z. Selden Jr.
CRHR: Archaeology
The East Texas Radiocarbon Database contributes to an analysis of tempo and place for Woodland era (~500 BC–AD 800) archaeological sites within the region. The temporal and spatial distributions of calibrated 14C ages (n = 127) with a standard deviation (ΔT) of 61 from archaeological sites with Woodland components (n = 51) are useful in exploring the development and geographical continuity of the peoples in east Texas, and lead to a refinement of our current chronological understanding of the period. While analysis of summed probability distributions (SPDs) produces less than significant findings due to sample size, they are used …
The East Texas Caddo: Modeling Tempo And Place, Robert Z. Selden Jr., Timothy K. Perttula
The East Texas Caddo: Modeling Tempo And Place, Robert Z. Selden Jr., Timothy K. Perttula
CRHR: Archaeology
Analysis of the Caddo sample (n=889 dates) from the East Texas radiocarbon database is used to establish the tempo and place of Caddo era (ca. A.D. 800-1680) archaeological sites, site clusters, and communities across the region. The temporal and spatial distribution of radiocarbon ages from settlements, mound centers, and cemeteries across the region have utility in exploring the development and geographical continuity of the Caddo peoples; establishing the specific times when areas were abandoned or population sizes diminished; and defining times and areas illustrating an intensification in mound center construction and large cemeteries became a focus of community social practices.
Carbon(Sp3)-Fluorine Bond-Forming Reductive Elimination From Palladium(Iv) Complexes., J. Brannon Gary
Carbon(Sp3)-Fluorine Bond-Forming Reductive Elimination From Palladium(Iv) Complexes., J. Brannon Gary
Faculty Publications
The development of transition-metal-catalyzed reactions for the formation of CF bonds has been an area of intense research over the past decade.[1–3] Traditionally, the CF coupling step of these sequences has proven challenging because of the high kinetic barrier for CF bond-forming reductive elimination from most transition-metal centers.[1] Our approach to address this challenge has involved the use of PdII catalysts in conjunction with F+-based oxidants. Since 2006, a variety of PdII-catalyzed reactions of F+ reagents have been developed to introduce fluorine at both C(sp2 ) and C(sp3 ) centers.[4–6] These transformations have been proposed to proceed through CF bond-forming …