Works matching DE "PHENYLENEDIAMINES"
Results: 1161
SYNTHESIS, STRUCTURE AND HIRSHFELD SURFACE ANALYSIS OF THE COMPLEX COMPOUND BASED ON Cd(II) SALT AND O-PHENYLENEDIAMINE.
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- Recent Contributions to Physics, 2024, v. 91, n. 4, p. 77, doi. 10.26577/RCPh.2024.v91.i4.a8
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STUDY OF FOULING AND MASS TRANSFER PROPERTIES OF CELLULOSE ACETATE-MODIFIED TFC MEMBRANES.
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- Cellulose Chemistry & Technology, 2024, v. 58, n. 9/10, p. 1177
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Allergic Contact Dermatitis to para-Phenylenediamine in Hair Dyes: New Insights.
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- Current Medical Literature: Dermatology, 2009, v. 14, n. 3, p. 57
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Contact allergy to para-phenylenediamine in a permanent eyelash dye.
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- Current Medical Literature: Dermatology, 2006, v. 11, n. 4, p. 101
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- Article
Fabrication of excellent anti-corrosion epoxy coating based on GON-An composites.
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- Surface Engineering, 2020, v. 36, n. 8, p. 877, doi. 10.1080/02670844.2020.1730061
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Sulfated Tin Oxide: An Immensely Potent and Reusable Catalyst for the Synthesis of Benzimidazole Derivatives.
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- Macromolecular Symposia, 2019, v. 387, n. 1, p. N.PAG, doi. 10.1002/masy.201800238
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Influence of Oxirane Ring and Phenylenediamine Structures in Modified Palm Processing Oils on Properties of ENR/PP TPVs.
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- Macromolecular Symposia, 2015, v. 354, n. 1, p. 21, doi. 10.1002/masy.201400070
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Molecular Simulation and Experimental Study on the Damping and Aging Properties of 4010NA/Hydrogenated Nitrile Butadiene/Nitrile Butadiene Rubber Composites.
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- Macromolecular Theory & Simulations, 2023, v. 32, n. 2, p. 1, doi. 10.1002/mats.202200072
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Ultraviolet Light Responsive N‐Nitroso Polymers for Antibacterial Nitric Oxide Delivery.
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- Macromolecular Rapid Communications, 2023, v. 44, n. 22, p. 1, doi. 10.1002/marc.202300473
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Enantioselective Construction of the Biologically Significant Dibenzo[1,4]diazepine Scaffold via Organocatalytic Asymmetric Three-Component Reactions.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 9, p. 2009, doi. 10.1002/adsc.201400095
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Laccase-Catalysed Homocoupling of Primary Aromatic Amines towards the Biosynthesis of Dyes.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 14/15, p. 2908, doi. 10.1002/adsc.201300501
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Quantum yield and photometric parameters of some transition metal ion schiff base complexes.
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- Optical & Quantum Electronics, 2017, v. 49, n. 9, p. 1, doi. 10.1007/s11082-017-1138-9
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The thermal behaviour of some Co(II) complex combinations with schiff bases.
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- Journal of Thermal Analysis & Calorimetry, 2003, v. 71, n. 2, p. 521
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DFT study of the condensation products of 2-chloro-3-formylquinolines with o-aminophenol, o-aminothiophenol and o-phenylenediamine.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2023, v. 142, n. 11, p. 1, doi. 10.1007/s00214-023-03052-2
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Theoretical and experimental investigation on the near-infrared and UV-vis spectral regions of a newly synthesized triarylamine electrochromic system.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2012, v. 131, n. 5, p. 1, doi. 10.1007/s00214-012-1225-8
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Stacking of triphenylene: characterization of the potential energy surface.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2010, v. 127, n. 3, p. 133, doi. 10.1007/s00214-009-0661-6
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Solid-Phase Synthesis of Oligo(triacetylene)s and Oligo(phenylenetriacetylene)s Employing Sonogashira and Cadiot—Chodkiewicz-Type Cross-Coupling Reactions.
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- Helvetica Chimica Acta, 2004, v. 87, n. 3, p. 698
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Opianic Acid in the Synthesis of Benzimidazole Derivatives.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 1, p. 118, doi. 10.1007/s10600-017-1923-5
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Synthesis of new N-aminoglycosides based on halo-substituted p-phenylenediamines and p-aminophenols.
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- Chemistry of Natural Compounds, 2009, v. 45, n. 4, p. 522, doi. 10.1007/s10600-009-9392-0
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Formation of 4-(het)aryl-3H-1,5-benzodiazepine-2-carboxylates from (het)aroylpyruvate esters and o-phenylenediamine.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 8, p. 574, doi. 10.1007/s10593-023-03235-6
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One-pot synthesis of 1,5-benzodiazepine-2,3-dicarboxylates via three-component domino reactions in the presence of γ-Fe<sub>2</sub>O<sub>3</sub>@SiO<sub>2</sub>/Ce(OTf)<sub>3</sub>.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 7/8, p. 806, doi. 10.1007/s10593-021-02984-6
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Synthesis of nitromethyl-, N-methylindolyl-, or N-methylindolylnitromethyl-substituted 1,4-benzothiazin(diazin)ones and 3-methyl-1,4-benzoxazinones from alkyl 3-nitroacrylates.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 7, p. 729, doi. 10.1007/s10593-018-2339-2
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Alkyl 3-bromo-3-nitroacrylates - convenient building blocks for the construction of benzo-fused six-membered N,N-, N,O- and five-membered O,O-heterocycles.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 5, p. 502, doi. 10.1007/s10593-018-2296-9
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Efficient Synthesis of Benzimidazoles Containing 1,2,4-Triazol-3-One Nucleus Using Microwave Technique.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 11, p. 948, doi. 10.1007/s10593-017-1991-2
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The rearrangement of trifluoroacetylchromenes to trifluoromethylchromenols.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 8, p. 559, doi. 10.1007/s10593-016-1931-6
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Synthesis of 6-Amino- and 6-Hydroxy-1-Aryl-2-(Thiazol-2-Yl)-9-(2-Thienoyl)-1,2-Dihydro-3 H-Pyrrolo[3,4- B]Quinolin-3-Ones.
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- Chemistry of Heterocyclic Compounds, 2015, v. 50, n. 12, p. 1692, doi. 10.1007/s10593-015-1639-z
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Preparation of 2-(1-adamantyl)-1 H-benzimidazole and novel derivatives thereof.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 2, p. 139, doi. 10.1007/s10593-015-1671-z
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Substituted 2-Formylbenzoic Acids in the Synthesis of 11<i>H</i>-Isoindolo[2,1-<i>a</i>]Benzimidazol-11-Ones, 5<i>H</i>-Isoindolo[2,1-<i>a</i>][3,1]Benzoxazine-5,11(6a<i>H</i>)-Diones, and 6,6a-Dihydroisoindolo-[2,1-<i>a</i>]Quinazoline-5,11-Diones.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 9, p. 1331, doi. 10.1007/s10593-013-1382-2
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Green Protocol: Solvent- and Catalyst-Free Synthesis of Benzimidazole Derivatives via Microwave Technique.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 8, p. 1136, doi. 10.1007/s10593-013-1354-6
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Benzazoles. 6*. Synthesis and Arylsulfonation of 2-Hydroxymethylbenzimidazole.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 5, p. 760, doi. 10.1007/s10593-013-1307-0
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Study of P-Phenylenediamine (PPD) Concentrations after Hair Dye Mixing: A Call for Safety Reassessment.
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- Cosmetics (2079-9284), 2022, v. 9, n. 2, p. 41, doi. 10.3390/cosmetics9020041
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Bio-Inspired Molecularly Imprinted Polymer Electrochemical Sensor for Cortisol Detection Based on O-Phenylenediamine Optimization.
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- Biomimetics (2313-7673), 2023, v. 8, n. 3, p. 282, doi. 10.3390/biomimetics8030282
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Para‐phenylenediamine deteriorates oocyte quality by impairing mitochondrial function.
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- Environmental Toxicology, 2022, v. 37, n. 7, p. 1803, doi. 10.1002/tox.23528
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para-Phenylenediamine induces apoptosis through activation of reactive oxygen species-mediated mitochondrial pathway, and inhibition of the NF-κB, m TOR, and Wnt pathways in human urothelial cells.
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- Environmental Toxicology, 2017, v. 32, n. 1, p. 265, doi. 10.1002/tox.22233
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Apoptosis induced by para-phenylenediamine involves formation of ROS and activation of p38 and JNK in chang liver cells.
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- Environmental Toxicology, 2014, v. 29, n. 9, p. 981, doi. 10.1002/tox.21828
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4-chloro-1,2-phenylenediamine Induces Apoptosis in Mardin-Darby canine kidney cells via activation of caspases.
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- Environmental Toxicology, 2014, v. 29, n. 6, p. 655, doi. 10.1002/tox.21792
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Remarkable Confinement Effect of Nanofiber in Carbon Nanotubes for Dehydrogenative Coupling of Alcohols with α‐Diaminobenzene: A Route for the Synthesis of Benzimidazoles.
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- ChemNanoMat, 2018, v. 4, n. 6, p. 542, doi. 10.1002/cnma.201700363
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New monomers with trifluoromethyl and phenylphosphine oxide substituents for polynaphthylimides and polyperyleneimides.
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- Doklady Chemistry, 2011, v. 440, n. 1, p. 248, doi. 10.1134/S0012500811090023
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Sampling and Analytical Method for Alpha-Dicarbonyl Flavoring Compounds via Derivatization with o-Phenylenediamine and Analysis Using GC-NPD.
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- Scientifica, 2016, p. 1, doi. 10.1155/2016/9059678
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Occupational eczema from N-isopropyl -N'-phenylparaphenylenediamine (IPPD) and N-dimethyl-1,3 butyl-N'-phenylparaphenylenediamine (DMPPD) in tyres.
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- Contact Dermatitis (01051873), 1977, v. 3, n. 1, p. 1, doi. 10.1111/j.1600-0536.1977.tb03580.x
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THE PERSISTENCE OF ALLERGIC ECZEMATOUS SENSITIVITY AND THE CROSS-SENSITIVITY PATTERN TO PARAPHENYLENEDIAMINE.
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- British Journal of Dermatology, 1959, v. 71, n. 7, p. 274
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A general population from Thailand: incidence of common allergens with emphasis on para-phenylenediamine.
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- Clinical & Experimental Allergy, 2007, v. 37, n. 12, p. 1848, doi. 10.1111/j.1365-2222.2007.02846.x
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p-Phenylenediamine allergy: the role of Bandrowski's base.
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- Clinical & Experimental Allergy, 2006, v. 36, n. 10, p. 1289, doi. 10.1111/j.1365-2222.2006.02561.x
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The clinical spectrum of reactions developed based on paraphenylenediamine hypersensitivity two pediatric cases.
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- Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2015, v. 32, n. 5, p. 393, doi. 10.5114/pdia.2015.52738
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Eosinophilic cellulitis (Wells' syndrome) caused by a temporary henna tattoo.
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- Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2014, v. 31, n. 5, p. 322, doi. 10.5114/pdia.2014.40951
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Surface Modification of Poly(biphenyl dianhydride-para-phenylene diamine) (BPDA-PDA) and Poly(pyromellitic dianhydride-oxydianiline) (PMDA-ODA) Polyimides with UV Photo-Oxidation.
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- Journal of Adhesion Science & Technology, 2010, v. 24, n. 6, p. 1153, doi. 10.1163/016942409X12598231568465
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Synthesis of cobalt complexes and their evaluation as an adhesion promoter in a rubber–steel wire system.
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- Journal of Adhesion Science & Technology, 2005, v. 19, n. 16, p. 1475, doi. 10.1163/156856105774805868
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Non-conventional synthesis and antibacterial activity of poly(aniline-co- o -phenylenediamine)/bentonite nanocomposites.
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- Designed Monomers & Polymers, 2014, v. 17, n. 5, p. 458, doi. 10.1080/15685551.2013.867570
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Synthesis and Characterization of Linear, Branched and Hyperbranched Triphenylamine-Based Polyazomethines.
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- Designed Monomers & Polymers, 2009, v. 12, n. 2, p. 177, doi. 10.1163/156855509X412117
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Graphene Aerogels for In Situ Synthesis of Conductive Poly(para-phenylenediamine) Polymers, and Their Sensor Application.
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- Atmosphere, 2020, v. 11, n. 7, p. 626, doi. 10.3390/mi11070626
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