Search Results - "Withey, Jonathan M"
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Depletion of hormones and antimicrobials in cattle manure using thermophilic anaerobic digestion
Published in Journal of chemical technology and biotechnology (1986) (01-09-2016)“…ABSTRACT BACKGROUND The fate and effect of hormone and antimicrobial residues in the manure of therapeutically treated cattle is of considerable concern…”
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Cross-Contamination of Ignitable Liquid Residues on Wildfire Debris—Effects of Packaging and Storage on Detection and Characterization
Published in Separations (01-02-2024)“…Producing defensible data for legal proceedings requires strict monitoring of sample integrity. In fire debris analysis, various approved packaging and storage…”
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Cross-Contamination of Ignitable Liquid Residues on Wildfire Debris—Detection and Characterization in Matrices Commonly Encountered at Wildfire Scenes
Published in Separations (01-09-2023)“…Ignitable liquid residue (ILR) samples play an important role in fire investigations. Similar to other types of forensic evidence, maintaining sample integrity…”
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Method development for optimizing analysis of ignitable liquid residues using flow-modulated comprehensive two-dimensional gas chromatography
Published in Journal of Chromatography A (25-10-2021)“…•Step-wise approach to method development for flow-modulated GC × GC–MS presented.•Detailed optimization of GC × GC hardware setup (column combination &…”
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Development of retention time indices for comprehensive multidimensional gas chromatography and application to ignitable liquid residue mapping in wildfire investigations
Published in Journal of Chromatography A (04-01-2021)“…In this study, we introduce a simple three-step workflow for a universally applicable RI system, to be used in GC×GC analysis of ignitable liquid residue (ILR)…”
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Enantioselective total synthesis of (R)-(-)-complanine
Published in Beilstein journal of organic chemistry (04-10-2012)“…A route is described for the enantioselective synthesis of (R)-(-)-complanine, a marine natural product isolated from Eurythoe complanata, and known to be a…”
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Operationally Simple Synthesis of N,N‑Diethyl-3-methylbenzamide (DEET) Using COMU as a Coupling Reagent
Published in Journal of chemical education (13-01-2015)“…A novel procedure is described where students use COMU [(1-cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate], as a…”
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Asymmetric synthesis of the cis- and trans-stereoisomers of 4-aminopyrrolidine-3-carboxylic acid and 4-aminotetrahydrofuran-3-carboxylic acid
Published in Organic & biomolecular chemistry (07-10-2004)“…The diastereoselective conjugate addition of lithium (S)-N-benzyl-N-[small alpha]-methylbenzylamide has been successfully applied to the first asymmetric…”
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Kinetic resolution of tert-butyl (RS)-3-alkylcyclopentene-1-carboxylates for the synthesis of homochiral 3-alkyl-cispentacin and 3-alkyl-transpentacin derivatives
Published in Organic & biomolecular chemistry (21-11-2004)“…High levels of stereocontrol are observed in the conjugate addition of lithium dibenzylamide to tert-butyl (RS)-3-alkylcyclopentene-1-carboxylates (alkyl = Et,…”
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Oxidative spirocyclisation routes towards the sawaranospirolides. Synthesis of ent-sawaranospirolides C and D
Published in Organic & biomolecular chemistry (01-01-2010)“…Two routes are described for the synthesis of the sawaranospirolides, stereoisomeric spirolactone ascorbigenins isolated from Chamaecyparis pisifera. Trapping…”
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Parallel kinetic resolution of tert-butyl (RS)-3-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 3-alkyl-cispentacin derivatives
Published in Organic & biomolecular chemistry (21-11-2004)“…The double mutual kinetic resolution of tert-butyl (RS)-3-benzyl-cyclopentene-1-carboxylate with a 50 : 50 mixture of lithium…”
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Strategies for the construction of morphinan alkaloid AB-rings: regioselective Friedel-Crafts-type cyclisations of γ-aryl-β-benzoylamido acids with asymmetrically substituted γ-aryl rings
Published in Tetrahedron: asymmetry (01-04-2016)“…[Display omitted] The regioselectivity of the Friedel-Crafts-type cyclisation of a range of γ-aryl-β-benzoylamido acids, bearing oxy substituents at the C(3)-…”
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