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1. Full Text Simultaneously enhanced production of poly(β‐malic acid) and pullulan using a dissolved oxygen shift (DO‐shift) control strategy
by Xia, Jun and Liu, Xiaoyan and Xu, Jiaxing and Xu, Jiming and Wang, Xingfeng and Li, Xiangqian
Journal of Chemical Technology & Biotechnology, ISSN 0268-2575, 06/2017, Volume 92, Issue 6, pp. 1464 - 1471
BACKGROUND Poly(β‐malic acid) (PMA) and pullulan are two valuable biopolymers that can be produced simultaneously by certain strains of pullulans. In previous... 
dissolved oxygen | pullulan | poly(malic acid) | co‐production | co-production | DRUG-DELIVERY | CHEMISTRY, MULTIDISCIPLINARY | EXOPOLYSACCHARIDE | ENGINEERING, CHEMICAL | ENGINEERING, ENVIRONMENTAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | AUREOBASIDIUM-PULLULANS | BIOSYNTHESIS | FERMENTATION | OPTIMIZATION | MALIC-ACID | POLYMALIC ACID | COPRODUCTION | Malic acid | Polysaccharides | Fermentation | Analysis | Pullulan | Acids | Saturation | Reaction kinetics | Strategy | Kinetics | Dissolved oxygen | Biopolymers
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2. Full Text DFT Study of the Mechanisms of In Water Au(I)-Catalyzed Tandem [3,3]-Rearrangement/Nazarov Reaction/[1,2]-Hydrogen Shift of Enynyl Acetates:  A Proton-Transport Catalysis Strategy in the Water-Catalyzed [1,2]-Hydrogen Shift
by Shi, Fu-Qiang and Li, Xin and Xia, Yuanzhi and Zhang, Liming and Yu, Zhi-Xiang
Journal of the American Chemical Society, ISSN 0002-7863, 12/2007, Volume 129, Issue 50, pp. 15503 - 15512
A computational study with the Becke3LYP density functional was carried out to elucidate the mechanisms of Au(I)-catalyzed reactions of enynyl acetates... 
EFFICIENT FORMATION | CYCLOADDITION REACTIONS | DIELS-ALDER REACTIONS | ALDOL REACTION | ORGANIC-REACTIONS | NAZAROV CYCLIZATION | GAS-PHASE | RADICAL CATIONS | FREE-ENERGIES | ATOM ABSTRACTION | CHEMISTRY, MULTIDISCIPLINARY | Density functionals | Usage | Gold compounds | Research | Chemical properties | Catalysis
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3. Full Text Pure shift NMR
by Zangger, Klaus
Progress in Nuclear Magnetic Resonance Spectroscopy, ISSN 0079-6565, 04/2015, Volume 86-87, pp. 1 - 20
Although scalar-coupling provides important structural information, the resulting signal splittings significantly reduce the resolution of NMR spectra. Limited... 
Pure shift NMR | Scalar coupling | NMR spectroscopy | Structure analysis | Homonuclear broadband decoupling | ONE-BOND COUPLINGS | RESIDUAL DIPOLAR COUPLINGS | SOLID-STATE NMR | NUCLEAR-MAGNETIC-RESONANCE | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | TWO-DIMENSIONAL NMR | CHEMISTRY, PHYSICAL | INTRINSICALLY DISORDERED PROTEINS | CONSTANT-TIME EVOLUTION | SPECTROSCOPY | HOMONUCLEAR BROAD-BAND | DIAGONAL PEAK SUPPRESSION | SPIN-SPIN SPLITTINGS | Carbon Isotopes | Proteins - analysis | Proteins - chemistry | Nuclear Magnetic Resonance, Biomolecular - methods | Nuclear magnetic resonance
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4. Full Text Combined chemical shift changes and amino acid specific chemical shift mapping of protein–protein interactions
by Schumann, Frank H and Riepl, Hubert and Maurer, Till and Gronwald, Wolfram and Neidig, Klaus-Peter and Kalbitzer, Hans Robert
Journal of Biomolecular NMR, ISSN 0925-2738, 12/2007, Volume 39, Issue 4, pp. 275 - 289
Protein–protein interactions are often studied by chemical shift mapping using solution NMR spectroscopy. When heteronuclear data are available the interaction... 
Biochemistry, general | Polymer Sciences | Biophysics/Biomedical Physics | NMR | Combined chemical shift | Chemical shift mapping | Physics | Protein–protein interaction | Protein-protein interaction | PHOSPHATASE HPTP1E | SITE | COMPLEX | CHYMOTRYPSIN | chemical shift mapping | BIOCHEMISTRY & MOLECULAR BIOLOGY | RAS-BINDING DOMAIN | PDZ2 DOMAIN | OVOMUCOID 3RD DOMAIN | ENZYME | SPECTROSCOPY | INHIBITOR | Protein Interaction Mapping - methods | Animals | Cattle | Sensitivity and Specificity | Amino Acids - chemistry | Chymotrypsin - chemistry | Nuclear Magnetic Resonance, Biomolecular | Protein Conformation | Ovomucin - chemistry | Nuclear magnetic resonance spectroscopy | Studies | Standard deviation | Nuclear magnetic resonance--NMR
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5. Full Text Increasing the Chemical‐Shift Dispersion of Unstructured Proteins with a Covalent Lanthanide Shift Reagent
by Göbl, Christoph and Resch, Moritz and Strickland, Madeleine and Hartlmüller, Christoph and Viertler, Martin and Tjandra, Nico and Madl, Tobias
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2016, Volume 55, Issue 47, pp. 14847 - 14851
The study of intrinsically disordered proteins (IDPs) by NMR often suffers from highly overlapped resonances that prevent unambiguous chemical‐shift... 
NMR | chemical-shift dispersion | pseudo-contact shifts | intrinsically disordered proteins | lanthanides | FUS | BACKBONE RESONANCE ASSIGNMENT | NMR-SPECTROSCOPY | UNFOLDED PROTEINS | CHEMISTRY, MULTIDISCIPLINARY | LOW-COMPLEXITY | BIOMOLECULAR NMR | REGIONS | TRANSPORTIN | BINDING | Magnetic Resonance Spectroscopy | Intrinsically Disordered Proteins - chemistry | Lanthanoid Series Elements - chemistry | Rare earth metals | Proteins | Cysteine | Information management | Analysis | Binding | Data analysis | Covalence | Nuclear magnetic resonance--NMR | Data processing | Dispersion | Complexity | Communications | Communication
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6. Full Text Selective measurement of 1H–1H scalar couplings from crowded chemical shift regions: Combined pure shift and spin‐echo modulation approach
by Kakita, Veera Mohana Rao and Jerripothula, Kanaka Mahalakshmi and Vemulapalli, Sahithya Phani Babu and Bharatam, Jagadeesh
Magnetic Resonance in Chemistry, ISSN 0749-1581, 10/2018, Volume 56, Issue 10, pp. 941 - 946
JHH scalar couplings carry rich structural information and their measurements are fundamental in the 1H NMR based elucidation of small and medium molecules,... 
spin‐echo modulation | 1H–1H J‐couplings | PSYCHE | homodecoupling | band‐selective refocusing | H J-couplings | band-selective refocusing | spin-echo modulation | Measurement | Analysis | Estrogen | Coupling (molecular) | Couplings | Testosterone | Organic chemistry | Chemical equilibrium | Sex hormones | Nuclear magnetic resonance--NMR | Spectral resolution
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7. Full Text A guide to small-molecule structure assignment through computation of (1 H and 13 C) NMR chemical shifts
by Willoughby, Patrick H and Jansma, Matthew J and Hoye, Thomas R
Nature Protocols, ISSN 1754-2189, 2014, Volume 9, Issue 3, pp. 643 - 660
This protocol is intended to provide chemists who discover or make new organic compounds with a valuable tool for validating the structural assignments of... 
ORGANIC-MOLECULES | STEREOISOMERS | DENSITY-FUNCTIONAL METHODS | NATURAL-PRODUCTS | STEREOCHEMISTRY | BIOCHEMICAL RESEARCH METHODS | HEXACYCLINOL | DIASTEREOISOMERS | Polycyclic Compounds - chemistry | Small Molecule Libraries - chemistry | Magnetic Resonance Spectroscopy | Models, Chemical | Epoxy Compounds - chemistry | Molecular Conformation | Organic Chemicals - chemistry | Molecular Structure | Spiro Compounds - chemistry | Usage | Research | Diastereomers | Spectrum analysis | Methods
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8. Full Text Solar‐Driven Water–Gas Shift Reaction over CuOx/Al2O3 with 1.1 % of Light‐to‐Energy Storage
by Zhao, Likuan and Qi, Yuhang and Song, Lizhu and Ning, Shangbo and Ouyang, Shuxin and Xu, Hua and Ye, Jinhua
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2019, Volume 58, Issue 23, pp. 7708 - 7712
Hydrogen production from coal gasification provides a cleaning approach to convert coal resource into chemical energy, but the key procedures of coal... 
CuOx | photocatalysis | water–gas shift (WGS) reaction | oxygen vacancy | photothermal catalysis | CuO | H-2 PRODUCTION | REDUCTION | CONVERSION | CO2 | MOSSBAUER | CHEMISTRY, MULTIDISCIPLINARY | water-gas shift (WGS) reaction | CATALYSTS | Coal conversion | Catalysis | Energy management systems | Force and energy | Gold | Energy consumption | Hydrogen storage | Hydrogen-based energy | Light irradiation | Catalysts | Radiation | Energy costs | Catalytic activity | Chemical energy | Aluminum oxide | Organic chemistry | Coal gasification | Energy technology | Energy | Thermal power | Platinum | Coal | Shift reaction | Irradiation | Hydrogen production | Energy storage
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9. Full Text Volumetric spiral chemical shift imaging of hyperpolarized [2‐13c]pyruvate in a rat c6 glioma model
by Park, Jae Mo and Josan, Sonal and Jang, Taichang and Merchant, Milton and Watkins, Ron and Hurd, Ralph E and Recht, Lawrence D and Mayer, Dirk and Spielman, Daniel M
Magnetic Resonance in Medicine, ISSN 0740-3194, 03/2016, Volume 75, Issue 3, pp. 973 - 984
Purpose MRS of hyperpolarized [2‐13C]pyruvate can be used to assess multiple metabolic pathways within mitochondria as the 13C label is not lost with the... 
hyperpolarized 13C | glioma | cancer | brain | [2‐13C]pyruvate | mitochondrial metabolism | C]pyruvate | hyperpolarized | PYRUVATE | hyperpolarized C-13 | DICHLOROACETATE | C-13 MAGNETIC-RESONANCE | IN-VIVO ASSESSMENT | DYNAMIC NUCLEAR-POLARIZATION | SPECTROSCOPY | METABOLISM | C-13-PYRUVATE | FATTY-ACID SYNTHASE | [2-C-13]pyruvate | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Neuroimaging - methods | Pyruvic Acid - chemistry | Rats, Wistar | Brain Neoplasms - pathology | Magnetic Resonance Imaging - methods | Rats | Male | Carbon Isotopes - metabolism | Image Processing, Computer-Assisted - methods | Brain - metabolism | Animals | Glioma - pathology | Brain - pathology | Pyruvic Acid - metabolism | Signal Processing, Computer-Assisted | Carbon Isotopes - chemistry | Lactates | Brain | Metabolites | Gliomas | Mitochondrial DNA | Glutamate | Carnitine | Neuroimaging | Dichloroacetic acid | Brain tumors | Muscles | Bicarbonates | Pyruvic acid | Metabolism | Kinases | Bearing | Artifacts | Bicarbonate | Organic chemistry | Chemical equilibrium | Mitochondria | Maps | Glioma | Magnetic resonance imaging | Metabolic pathways | Lactic acid | Tumors | [2-13C]pyruvate
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10. NMR shift reagents
by Wenzel, Thomas J
1987, ISBN 9780849352980, 286
Lanthanide shift reagents | Nuclear magnetic resonance spectroscopy | Stereochemistry
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11. Full Text Measuring the Brønsted acid strength of zeolites-does it correlate with the O-H frequency shift probed by a weak base?
by Arean, Carlos O and Delgado, Montserrat R and Nachtigall, Petr and Thang, Ho Viet and Rubeš, Miroslav and Bulánek, Roman and Chlubná-Eliášová, Pavla
Physical Chemistry Chemical Physics, ISSN 1463-9076, 06/2014, Volume 16, Issue 21, pp. 10129 - 10141
Bronsted-acid zeolites are currently being used as catalysts in a wide range of technological processes, spanning from the petrochemical industry to biomass... 
77 K | CARBON-MONOXIDE | CATALYTIC-PROPERTIES | CO ADSORPTION | Y ZEOLITE | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | TEMPERATURE INFRARED-SPECTROSCOPY | CHEMISTRY, PHYSICAL | BASIS-SETS | DIATOMIC MOLECULAR PROBES | BRIDGING HYDROXYLS | AMINE TITRATION
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