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1. Full Text Catalysis with N‐Heterocyclic Carbenes under Oxidative Conditions
by De Sarkar, Suman and Biswas, Anup and Samanta, Ramesh C and Studer, Armido
Chemistry – A European Journal, ISSN 0947-6539, 04/2013, Volume 19, Issue 15, pp. 4664 - 4678
This Concept article discusses the potential of oxidative carbene catalysis in synthesis and comprehensively covers pioneering studies as well as recent... 
cascade reactions | organocatalysis | carbenes | biomimetic catalysis | umpolung | ACTIVE ALDEHYDES | DIELS-ALDER REACTIONS | ALPHA,BETA-UNSATURATED ALDEHYDES | THIAMINE-DEPENDENT ENZYMES | PYRUVATE-FERREDOXIN OXIDOREDUCTASE | AROMATIC-ALDEHYDES | ALPHA-KETO ACIDS | CHEMISTRY, MULTIDISCIPLINARY | AEROBIC CONDITIONS | RADICAL INTERMEDIATE | CATIONIC MICELLE | Biomimetics | Pyridine | Catalysis | Synthesis | Oxidants | Cascades | Oxidizing agents | Nucleophiles | Aldehydes | Carbenes
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2. Full Text Highly Efficient CH Hydroxylation of Carbonyl Compounds with Oxygen under Mild Conditions
by Liang, Yu‐Feng and Jiao, Ning
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2014, Volume 53, Issue 2, pp. 548 - 552
A transition‐metal‐free Cs2CO3‐catalyzed α‐hydroxylation of carbonyl compounds with O2 as the oxygen source is described. This reaction provides an efficient... 
oxygenation | cesium | dioxygen | CH functionalization | hydroxylation | C-H functionalization | ORGANIC-CHEMICALS | 1,3-DICARBONYL COMPOUNDS | BOND FORMATION | CHEMISTRY, MULTIDISCIPLINARY | KETONES | AEROBIC OXYGENATION | ELECTRON-TRANSFER | CH functionalization | ALPHA-HYDROXYLATION | PALLADIUM-CATALYZED OXIDATION | SINGLET OXYGEN | MOLECULAR-OXYGEN | Carbamates - chemical synthesis | Hydrogen Bonding | Hydroxylation | Oxygen - chemistry | Molecular Structure | Catalysis | Carbamates - chemistry | Carbonyl compounds | Oxidants | Oxidizing agents | Cleavage | Transformations | Bonding | Pharmaceuticals
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3. Full Text From model studies on Au(111) to working conditions with unsupported nanoporous gold catalysts: Oxygen-assisted coupling reactions
by Stowers, K.J and Madix, R.J and Friend, C.M
Journal of Catalysis, ISSN 0021-9517, 12/2013, Volume 308, pp. 131 - 141
Model studies on metallic single crystal gold provide principles for understanding and improving similar oxidation reactions on nanoporous gold-silver alloys.... 
Gold | Heterogeneous catalysis | Oxygen activation | Reaction mechanism | Oxidation | Catalysis | Nanoporous | Metal alloys | SELECTIVE OXIDATION | METHANOL | STABILITY | CHEMISTRY, PHYSICAL | AU-PD ALLOY | LIQUID-PHASE | ENGINEERING, CHEMICAL | CARBON-MONOXIDE | ATOMIC OXYGEN | TEMPERATURE CO OXIDATION | AEROBIC OXIDATION | SURFACE-CHEMISTRY
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4. Full Text Iron-catalyzed oxidative functionalization of C(sp(3))-H bonds under bromide-synergized mild conditions
by Yu, H and Zhao, QX and Wei, ZY and Wu, ZK and Li, Q and Han, S and Wei, YG
CHEMICAL COMMUNICATIONS, ISSN 1359-7345, 07/2019, Volume 55, Issue 54, pp. 7840 - 7843
An efficient oxidation and functionalization of C-H bonds with an inorganic-ligand supported iron catalyst and hydrogen peroxide to prepare the corresponding... 
OXYGEN | ACTIVATION | POLYOXOMETALATE | C-H OXIDATION | AEROBIC OXIDATION | REMOTE | CHEMISTRY, MULTIDISCIPLINARY
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5. Full Text Iodine(III)-mediated intermolecular allylic amination under metal-free conditions
by Souto, José A and Zian, Debora and Muñiz, Kilian
Journal of the American Chemical Society, ISSN 0002-7863, 05/2012, Volume 134, Issue 17, pp. 7242 - 7245
A new approach to direct intermolecular allylic amination has been developed using metal-free conditions at room temperature. The reaction employs a... 
FUNCTIONALIZATION | AEROBIC OXIDATIVE AMINATION | HYPERVALENT IODINE | POLYVALENT IODINE COMPOUNDS | MEDIATED AZIRIDINATION | AMBIENT-TEMPERATURE | N BOND FORMATION | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | C-H AMINATION | TERMINAL ALKENES | Chemical bonds | Iodine compounds | Allylic compounds | Amines | Chemical properties | Analysis
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6. Full Text Nanomagnetic organic–inorganic hybrid (Fe@Si-Gu-Prs): a novel magnetically green catalyst for the synthesis of tetrahydropyridine derivatives at room temperature under solvent-free conditions
by Eshghi, Hossein and Khojastehnezhad, Amir and Moeinpour, Farid and Rezaeian, Shima and Bakavoli, Mehdi and Teymouri, Mohsen and Rostami, Amin and Haghbeen, Kamahldin
Tetrahedron, ISSN 0040-4020, 01/2015, Volume 71, Issue 3, pp. 436 - 444
A novel nanomagnetic organic–inorganic hybrid catalyst (Fe@Si-Gu-Prs) was prepared by the chemical anchoring of Preyssler heteropolyacid (H [NaP W O ]) onto... 
Fe3O4 | Nanomagnetic catalyst | Preyssler | Heteropolyacid | Organic–inorganic hybrid | Organic-inorganic hybrid | Preyssler Fe | ONE-POT SYNTHESIS | FERRITE NANOPARTICLES | CHEMISTRY, ORGANIC | NANOPARTICLE-SUPPORTED GUANIDINE | 1ST APPLICATION | REUSABLE CATALYST | HETEROPOLY ACIDS | AEROBIC OXIDATION | SILICA-COATED NIFE2O4 | HETEROGENEOUS CATALYST | PD CATALYST | Genetic engineering | Nanoparticles | Synthesis (chemistry) | Inductively coupled plasma | Transmission electron microscopy | Catalysts | Nanostructure | Derivatives | Dispersion
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7. Full Text Pd/C‐Catalyzed Cyclizative Cross‐Coupling of Two ortho‐Alkynylanilines under Aerobic Conditions: Synthesis of 2,3′‐Bisindoles
by Yao, Bo and Wang, Qian and Zhu, Jieping
Chemistry – A European Journal, ISSN 0947-6539, 05/2015, Volume 21, Issue 20, pp. 7413 - 7416
A palladium‐catalyzed cyclizative cross‐coupling of two o‐alkynylanilines to 2,3′‐bisindoles under aerobic oxidative conditions was developed. Mechanistic... 
bisindoles | cyclizative cross‐coupling | o‐alkynylaniline | palladium | aerobic oxidative conditions | O-alkynylaniline | Aerobic oxidative conditions | Cyclizative cross-coupling | Palladium | Bisindoles | EFFICIENT SYNTHESIS | TERMINAL ALKYNES | DIMERIZATION | cyclizative cross-coupling | o-alkynylaniline | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | H FUNCTIONALIZATION | HETEROCYCLES | TANDEM REACTION | OXIDATIVE CYCLIZATION | DERIVATIVES | ALKALOIDS | Consumption | Cross coupling | Catalysts | Chemical reactions | Formations | Transformations | Catalysis
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8. Full Text Candidatus Accumulibacter gene expression in response to dynamic EBPR conditions
by He, Shaomei and McMahon, Katherine D
ISME Journal, ISSN 1751-7362, 02/2011, Volume 5, Issue 2, pp. 329 - 340
Enhanced biological phosphorus removal (EBPR) activated sludge communities enriched in 'Candidatus Accumulibacter' relatives are widely used in wastewater... 
Enhanced biological phosphorus removal | candidatus accumulibacter | RT-qPCR | gene expression | BIOCHEMICAL-MODEL | ACTIVATED-SLUDGE | ACCUMULATING ORGANISMS | ESCHERICHIA-COLI | MICROBIOLOGY | PHOSPHATE REMOVAL | AEROBIC CONDITIONS | enhanced biological phosphorus removal | WASTE-WATER | POLYPHOSPHATE KINASE | ECOLOGY | SEQUENCING BATCH REACTOR | BIOLOGICAL PHOSPHORUS REMOVAL | Anaerobiosis | Phosphates - metabolism | Genes, Bacterial - genetics | Phosphorus - metabolism | Acetates - metabolism | Betaproteobacteria - metabolism | Gene Expression Profiling | Gene Expression Regulation, Bacterial | Acetyl Coenzyme A - metabolism | Oxygen - metabolism | Sewage - microbiology | Betaproteobacteria - genetics | Original
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9. Full Text Gold Nanoparticle–Polydopamine–Reduced Graphene Oxide Ternary Nanocomposite as an Efficient Catalyst for Selective Oxidation of Benzylic C(sp3)−H Bonds Under Mild Conditions
by Majumdar, Biju and Bhattacharya, Tamalika and Sarma, Tridib K
ChemCatChem, ISSN 1867-3880, 05/2016, Volume 8, Issue 10, pp. 1825 - 1835
A ternary nanocomposite comprising of Au nanoparticles (NPs), polydopamine, and reduced graphene oxide exhibits excellent activity and selectivity towards the... 
oxidation | nanoparticles | heterogeneous catalysis | supported catalysts | graphene | Nanoparticles | Supported catalysts | Heterogeneous catalysis | Oxidation | Graphene | HYDROGEN ABSTRACTION | ALKANE OXIDATION | CHEMISTRY, PHYSICAL | PD ALLOY NANOPARTICLES | HYDROCARBON OXIDATION | C-H BONDS | VISIBLE-LIGHT | ELECTRON-TRANSFER | N-HYDROXYPHTHALIMIDE NHPI | AEROBIC OXIDATION | MOLECULAR-OXYGEN | Oxidation-reduction reaction | Chemical properties | Graphite
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10. Full Text Direct Production of (R)‐3‐Hydroxybutyric Acid of High Optical Purity by Halomonas sp. OITC1261 Under Aerobic conditions
by Yokaryo, Hiroto and Teruya, Morimi and Hanashiro, Ryuji and Goda, Masahiro and Tokiwa, Yutaka
Biotechnology Journal, ISSN 1860-6768, 02/2018, Volume 13, Issue 2, pp. 1700343 - n/a
The chiral compound (R)‐3‐hydroxybutyric acid (R‐3HB) has some important physiological functions in the human body and can also be applied as a functional... 
fermentation | Halomonas | sucrose | aerobic culture | 3‐hydroxybutyric acid | 3-hydroxybutyric acid | RECOMBINANT ESCHERICHIA-COLI | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ALCALIGENES-EUTROPHUS | BIOCHEMICAL RESEARCH METHODS
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11. Full Text Transforming CdS into an efficient visible light photocatalyst for selective oxidation of saturated primary C-H bonds under ambient conditions
by Zhang, Yanhui and Zhang, Nan and Tang, Zi-Rong and Xu, Yi-Jun
Chemical Science, ISSN 2041-6520, 09/2012, Volume 3, Issue 9, pp. 2812 - 2822
Selective activation of saturated sp(3) C-H bonds to high-value-added chemicals remains a significant but challenging task for the sustainable exploitation of... 
TIO2 PHOTOCATALYSIS | AROMATIC ALCOHOLS | MOLECULAR-SIEVE CATALYSTS | METHYL-ORANGE | GAS-PHASE | HYDROGEN-PRODUCTION | AEROBIC OXIDATION | SEMICONDUCTOR PHOTOCATALYSIS | CORRESPONDING ALDEHYDES | TITANIUM-DIOXIDE | CHEMISTRY, MULTIDISCIPLINARY | Oxidants | Semiconductors | Photocatalysis | Cadmium sulfides | Chemical bonds | Activation | Oxidation | Selectivity
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12. Full Text Double‐Oxidative Dehydrogenative (DOD) Cyclization of Glycine Derivatives with Dioxane under Metal‐Free Aerobic Conditions
by Huo, Congde and Xie, Haisheng and Chen, Fengjuan and Tang, Jing and Wang, Yajun
Advanced Synthesis & Catalysis, ISSN 1615-4150, 03/2016, Volume 358, Issue 5, pp. 724 - 730
The first carbon tetrabromide‐promoted novel double‐oxidative dehydrogenative cyclization/acidic ring opening/aromatization tandem reaction of glycine... 
aerobic conditions | carbon tetrabromide (CBr4) | oxidative coupling | dioxane | glycine derivatives | carbon tetrabromide (CBr | AMINO CARBONYL-COMPOUNDS | C BOND FORMATION | VISIBLE-LIGHT PHOTOREDOX | STRUCTURALLY DIVERSE | ARYLATION | CHEMISTRY, ORGANIC | CATALYTIC AMOUNTS | ELECTRON-TRANSFER | COUPLING REACTION | TRANSITION-METAL | H BONDS | CHEMISTRY, APPLIED | Quinoline | Glycine | Dioxane | Synthesis | Dehydrogenation | Derivatives |