0000000000134004

AUTHOR

Barbara Riehl

showing 7 related works from this author

Dynamic Precision Phenotyping Reveals Mechanism of Crop Tolerance to Root Herbivory.

2016

The western corn rootworm (WCR; Diabrotica virgifera virgifera LeConte) is a major pest of maize (Zea mays) that is well adapted to most crop management strategies. Breeding for tolerance is a promising alternative to combat WCR but is currently constrained by a lack of physiological understanding and phenotyping tools. We developed dynamic precision phenotyping approaches using 11C with positron emission tomography, root autoradiography, and radiometabolite flux analysis to understand maize tolerance to WCR. Our results reveal that WCR attack induces specific patterns of lateral root growth that are associated with a shift in auxin biosynthesis from indole-3-pyruvic acid to indole-3-aceton…

0106 biological sciences0301 basic medicineCrops AgriculturalIndolesPhysiologyGlutamineResearch Articles - Focus IssuePlant Science580 Plants (Botany)01 natural sciencesPlant RootsZea maysHost-Parasite InteractionsCrop03 medical and health sciencesBotanyGeneticsAnimalsCarbon RadioisotopesHerbivoryAmino AcidsPlant DiseasesHerbivorebiologyIndoleacetic AcidsMechanism (biology)Lateral rootfungifood and beveragesBiological Transportbiology.organism_classificationZea maysColeoptera030104 developmental biologyWestern corn rootwormPhenotypeAgronomyPositron-Emission TomographyPEST analysisFlux (metabolism)010606 plant biology & botanyPlant physiology
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Synthesis of l -[4-11 C]Asparagine by Ring-Opening Nucleophilic 11 C-Cyanation Reaction of a Chiral Cyclic Sulfamidate Precursor

2018

The development of a convenient and rapid method to synthesize radiolabeled, enantiomerically pure amino acids (AAs) as potential positron emission tomography (PET) imaging agents for mapping various biochemical transformations in living organisms remains a challenge. This is especially true for the synthesis of carbon-11-labeled AAs given the short half-life of carbon-11 (11 C, t1/2 =20.4 min). A facile synthetic pathway to prepare enantiomerically pure 11 C-labeled l-asparagine was developed using a partially protected serine as a starting material with a four-step transformation providing a chiral five-membered cyclic sulfamidate as the radiolabeling precursor. Its structure and absolute…

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryAbsolute configurationStereoisomerismGeneral ChemistryCyanation010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesAmino acidHydrolysisNucleophilechemistryYield (chemistry)AsparagineChemistry - A European Journal
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Electro-organic Synthesis as a Sustainable Alternative for Dehydrogenative Cross-Coupling of Phenols and Naphthols

2016

The dehydrogenative cross-coupling of phenols and naphthols can be achieved by several oxidative methods. However, the key is the use of fluorinated alcohols such as 1,1,1,3,3,3-hexafluoroisopropanol. The direct application of electricity represents an alternative synthetic approach, which is superior to other oxidizers (e.g., peroxides). The method is sustainable, inherently safe, and easily scalable.

Chemical substance010405 organic chemistryChemistryAnodic oxidationOrganic Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCoupling (computer programming)Organic chemistryOrganic synthesisPhenolsSynthesis
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A solvent-directed stereoselective and electrocatalytic synthesis of diisoeugenol.

2018

A stereoselective and electrocatalytic coupling reaction of isoeugenol has been reported for the first time in a 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP)/boron-doped diamond (BDD) electrode system. This particular C-C bond formation and diastereoselectivity is driven by a solvate interaction between the radical species and another isoeugenol molecule. Due to an electrocatalytic cycle, only understoichiometric amounts of charge are necessary. Since electric current is directly employed as the oxidant, the reaction is metal and reagent-free. In addition, the electrolysis can be conducted in a very simple undivided beaker-type cell under constant current conditions. Therefore, the protocol is …

010402 general chemistry01 natural sciencesCatalysisCoupling reactionlaw.inventionMetalchemistry.chemical_compoundlawMaterials ChemistryMoleculeElectrolysis010405 organic chemistryMetals and AlloysGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventIsoeugenolchemistryvisual_artElectrodeCeramics and Compositesvisual_art.visual_art_mediumStereoselectivityChemical communications (Cambridge, England)
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Unexpected high robustness of electrochemical cross-coupling for a broad range of current density

2017

Solvent effect enables electrosynthesis of organic compounds with strong variation of electric current at constant efficacy.

CouplingMultidisciplinaryMaterials science010405 organic chemistrySciAdv r-articlesNanotechnologyElectrolyte010402 general chemistry01 natural sciences0104 chemical sciencesAnodeChemical physicsRobustness (computer science)Yield (chemistry)ElectrochemistryConstant currentCurrent densityOrder of magnitudeResearch ArticlesResearch ArticleScience Advances
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Electrochemical Arylation Reaction

2018

Arylated products are found in various fields of chemistry and represent essential entities for many applications. Therefore, the formation of this structural feature represents a central issue of contemporary organic synthesis. By the action of electricity the necessity of leaving groups, metal catalysts, stoichiometric oxidizers, or reducing agents can be omitted in part or even completely. The replacement of conventional reagents by sustainable electricity not only will be environmentally benign but also allows significant short cuts in electrochemical synthesis. In addition, this methodology can be considered as inherently safe. The current survey is organized in cathodic and anodic con…

010405 organic chemistryReducing agentGeneral Chemistry010402 general chemistryElectrochemistrySustainable process01 natural sciencesCombinatorial chemistry0104 chemical sciencesAnodeCathodic protectionchemistry.chemical_compoundchemistryReagentOrganic synthesisMetal catalystChemical Reviews
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CCDC 1415388: Experimental Crystal Structure Determination

2018

Related Article: Youwen Xu, Aylin Sibel Cankaya, Ruma Hoque, So Jeong Lee, Colleen Shea, Lena Kersting, Michael Schueller, Joanna S. Fowler, David Szalda, David Alexoff, Barbara Riehl, Tassilo Gleede, Richard A. Ferrieri, Wenchao Qu|2018|Chem.-Eur.J.|24|6848|doi:10.1002/chem.201801029

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersdi-t-butyl 123-oxathiazolidine-34-dicarboxylate 22-dioxideExperimental 3D Coordinates
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