Works matching DE "ORGANIC compound derivatives"
Results: 103
Modified Coumarins. 33. Synthesis of Furo- and Dihydropyranocoumarins Containing a Lupinine Moiety.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 5, p. 815, doi. 10.1007/s10600-015-1423-4
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Reactions of 1-substituted 8-hydrazinotheobromines with Dicarbonyl Compounds.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 6, p. 1066, doi. 10.1007/s10600-014-1160-0
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Recent advances in the synthesis and synthetic applications of 1,2,3-triazoles (microreview).
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 3, p. 314, doi. 10.1007/s10593-018-2265-3
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[InlineMediaObject not available: see fulltext.]Alkylidene and arylidene Meldrum's acids as versatile reagents for the synthesis of heterocycles.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 1, p. 7, doi. 10.1007/s10593-016-1822-x
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Grinding-induced synthesis of heterocyclic fullerene derivatives under solvent-free conditions.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 1, p. 39, doi. 10.1007/s10593-015-1657-x
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Reduction of 7-R derivatives of 7 H-tris[1,2,5]oxa-diazolo[3,4- b:3′,4′- d:3″,4″- f]azepine 1-oxide with furoxan ring opening. preparation of 4-R-4 H-bis-[1,2,5]oxadiazolo[3,4- b:3′,4′- f]azepine-8,9-diamines.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 7, p. 1068, doi. 10.1007/s10593-013-1345-7
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An efficient synthesis of ferrocenyl-containing 1,3,4-oxadiazole derivatives via oxidative cyclization reaction.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 7, p. 1061, doi. 10.1007/s10593-013-1344-8
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PEG-400 as an efficient and recyclable reaction medium for the synthesis of polyhydroquinolines via Hantzsch reaction.
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- Orbital: The Electronic Journal of Chemistry, 2012, v. 4, n. 4, p. 245
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Synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] and spiro[indoline-3,4′-pyrano[2,3-c]chromene] derivatives using silica-bonded ionic liquids as a recyclable catalyst in aqueous medium.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 5, p. 859, doi. 10.1007/s13738-015-0801-y
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Iranian chemist's efforts to provide various effective methods for the synthesis of xanthenes.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 3, p. 791, doi. 10.1007/s13738-013-0353-y
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Recent Progress in the in situ Detrifluoroacetylative Generation of Fluoro Enolates and Their Reactions with Electrophiles.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 29, p. 6401, doi. 10.1002/ejoc.201500787
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Selective Production of Carbon Monoxide via Methane Oxychlorination over Vanadyl Pyrophosphate.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 50, p. 15619, doi. 10.1002/anie.201608165
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New Isolated-Pentagon-Rule and Skeletally Transformed Isomers of C<sub>100</sub> Fullerene Identified by Structure Elucidation of their Chloro Derivatives.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 10, p. 3451, doi. 10.1002/anie.201511928
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Crystal structure of 1,3-bis(6-methoxyquinolin-2-yl)benzene, C<sub>26</sub>H<sub>20</sub>N<sub>2</sub>O<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2013, v. 228, n. 3, p. 371, doi. 10.1524/ncrs.2013.0184
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Crystal structure of 3-(p-bromobenzoyl)-4-(p-bromophenyl)-1-isopropyl-4-piperidinol hydrochloride, C<sub>21</sub>H<sub>24</sub>Br<sub>2</sub>ClNO<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2013, v. 228, n. 3, p. 381, doi. 10.1524/ncrs.2013.0190
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Crystal structure of (benzoylacetonato-κ<sup>2</sup>O,O')dichloridodimethoxidotantalum(V), C<sub>12</sub>H<sub>15</sub>Cl<sub>2</sub>O<sub>4</sub>Ta.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2013, v. 228, n. 3, p. 397, doi. 10.1524/ncrs.2013.0200
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Starch Derivatives Bearing Aromatic Sulfonated Functional Groups.
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- Starch / Staerke, 2018, v. 70, n. 3/4, p. 1, doi. 10.1002/star.201700229
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Synthesis and Antibacterial Activity of 3,6-Diaryl-7 H-[1,2,4]Triazolo[3,4- b][1,3,4]Thiadiazines.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 1, p. 10, doi. 10.1007/s11094-016-1389-y
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Synthesis of New 1,3,4-Thiadiazines Capable of Inhibiting Nonenzymatic Glycosylation of Proteins.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 8, p. 501, doi. 10.1007/s11094-015-1314-9
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PAH and IUPAC Nomenclature.
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- Polycyclic Aromatic Compounds, 2015, v. 35, n. 2-4, p. 161, doi. 10.1080/10406638.2014.918551
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Bromination of adamantane and its derivatives with tetrabromomethane catalyzed by iron compounds.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 2, p. 184, doi. 10.1134/S1070428015020074
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Wittig rearrangement of 1-[(1 E)-3-(Benzyloxy)prop-1-en-1-yl]adamantane.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 9, p. 1268, doi. 10.1134/S107042801409005X
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Adamantylation of carbonitriles with 1,3-dehydroadamantane and its homologs.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 9, p. 1279, doi. 10.1134/S1070428014090085
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Synthesis of the first organylcyclosiloxane containing a benzimidazole fragment in the cycle.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 9, p. 1377, doi. 10.1134/S1070428014090255
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Zwitter-ionic structure of diethoxyfurotropylium dimethylbarbiturate.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 8, p. 1223, doi. 10.1134/S1070428014080302
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Iron-Catalyzed Carbonyl–Alkyne and Carbonyl–Olefin Metathesis Reactions.
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- Catalysts (2073-4344), 2020, v. 10, n. 9, p. 1092, doi. 10.3390/catal10091092
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Bioconversion of acrylonitrile using nitrile hydratase activity of <italic>Bacillus</italic> sp. APB-6.
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- 3 Biotech, 2018, v. 8, n. 5, p. 1, doi. 10.1007/s13205-018-1207-1
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Electro-generation of NaOH-H<sub>2</sub>SO<sub>4</sub> and simultaneous degradation of Acid orange 7 from Na<sub>2</sub>SO<sub>4</sub>-containing wastewater by Ti/ IrO<sub>2</sub> electrodes.
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- Journal of Chemical Technology & Biotechnology, 2017, v. 92, n. 4, p. 827, doi. 10.1002/jctb.5066
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Synthesis and Study of Some New Quinolone Derivatives Containing a 3-acetyl Coumarin for Their Antibacterial and Antifungal Activities.
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- Iranian Journal of Pharmaceutical Research, 2017, v. 16, n. 2, p. 554
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Nucleoside Analogues: Synthesis and Biological Properties of Azanucleoside Derivatives (Eur. J. Org. Chem. 11/2014).
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 11, p. n/a, doi. 10.1002/ejoc.201490027
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- Article
Synthesis and In Vitro Antibacterial Activities of Novel 2-Aryl-3-(phenylamino)-2,3-dihydroquinazolin-4(1 H)-one Derivatives.
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- Journal of Heterocyclic Chemistry, 2013, v. 50, n. 5, p. 1129, doi. 10.1002/jhet.1075
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Photoredox-Catalyzed Dimerization of Arylalkenes via an Oxidative [4+2] Cycloaddition Sequence: Synthesis of Naphthalene Derivatives.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 23, p. 3887, doi. 10.1002/adsc.201600587
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Prediction of soil organic carbon at the country scale: stratification strategies for near-infrared data.
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- European Journal of Soil Science, 2017, v. 68, n. 6, p. 919, doi. 10.1111/ejss.12485
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Quantitative analysis of the therapeutic effect of magnolol on MPTP-induced mouse model of Parkinson’s disease using in vivo <sup>18</sup>F-9-fluoropropyl-(+)-dihydrotetrabenazine PET imaging.
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- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173503
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Biodegradation of nitroaromatic compounds in Red Water by white rot fungi Pleurotus ostreatus and floridae.
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- Revista Ambiente e Água, 2020, v. 15, n. 6, p. 1, doi. 10.4136/ambi-agua.2594
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An anionic two-dimensional indium carboxylate framework derived from a pseudo C-symmetric semi-flexible tricarboxylic acid.
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- Journal of Chemical Sciences, 2014, v. 126, n. 5, p. 1385, doi. 10.1007/s12039-014-0676-y
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Low Mass Ions in Laser Desorption/Ionization Mass Spectrometry of 1-Methoxy-5-aminotetrazole.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 1, p. 99, doi. 10.1002/bkcs.10612
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Enantiopure Sulfinyl Aniline as a Removable and Recyclable Chiral Auxiliary for Asymmetric C(sp<sup>3</sup>)−H Bond Activation.
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- Chemistry - A European Journal, 2016, v. 22, n. 48, p. 17397, doi. 10.1002/chem.201603507
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Towards Safer Rocket Fuels: Hypergolic Imidazolylidene-Borane Compounds as Replacements for Hydrazine Derivatives.
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- Chemistry - A European Journal, 2016, v. 22, n. 29, p. 10187, doi. 10.1002/chem.201601343
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n-Dopants Based on Dimers of Benzimidazoline Radicals: Structures and Mechanism of Redox Reactions.
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- Chemistry - A European Journal, 2015, v. 21, n. 30, p. 10878, doi. 10.1002/chem.201500611
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Highly Functionalized Cyclopentane Derivatives by Tandem Michael Addition/Radical Cyclization/Oxygenation Reactions.
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- Chemistry - A European Journal, 2015, v. 21, n. 27, p. 9877, doi. 10.1002/chem.201500424
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HOMO Stabilisation in π-Extended Dibenzotetrathiafulvalene Derivatives for Their Application in Organic Field-Effect Transistors.
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- Chemistry - A European Journal, 2014, v. 20, n. 50, p. 16672, doi. 10.1002/chem.201404508
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Disrupting VEGF-VEGFR1 Interaction: De Novo Designed Linear Helical Peptides to Mimic the VEGF<sub>13-25</sub> Fragment.
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- Molecules, 2017, v. 22, n. 11, p. 1846, doi. 10.3390/molecules22111846
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Design, Synthesis and Bioactivity Evaluation of Novel β-carboline 1,3,4-oxadiazole Derivatives.
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- Molecules, 2017, v. 22, n. 11, p. 1811, doi. 10.3390/molecules22111811
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Selective and Efficient Generation of ortho-Brominated para-Substituted Phenols in ACS-Grade Methanol.
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- Molecules, 2016, v. 21, n. 1, p. 88, doi. 10.3390/molecules21010088
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Synthesis and Antiviral Activity of N-Phenylbenzamide Derivatives, a Novel Class of Enterovirus 71 Inhibitors.
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- Molecules, 2013, v. 18, n. 3, p. 3630, doi. 10.3390/molecules18033630
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- Article
Energetic and Structural Studies of Two Biomass-Derived Compounds: 6- and 7-hydroxy-1-indanones.
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- Applied Sciences (2076-3417), 2020, v. 10, n. 23, p. 8512, doi. 10.3390/app10238512
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Green Production of Indolylquinones, Derivatives of Perezone, and Related Molecules, Promising Antineoplastic Compounds.
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- Journal of Chemistry, 2016, p. 1, doi. 10.1155/2016/3870529
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Group Separation of Water-soluble Organic Carbon Fractions in Ash Samples from a Coal Combustion Boiler.
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- Asian Journal of Atmospheric Environment (AJAE), 2012, v. 6, n. 1, p. 67, doi. 10.5572/ajae.2012.6.1.067
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Quick and Convenient Comparison of Curry Powders Using Direct Thermal Desorption with GC-MS Analysis.
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- LC-GC Europe, 2015, v. 28, n. 12, p. 684
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