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1. Full Text Effects of interaction between the chelate rings and [pi]-conjugated systems in fused salphen complexes on UV-Vis-NIR spectra
by Hirohiko Houjou and Keisuke Yagi and Isao Yoshikawa and Toshiki Mutai and Koji Araki
Journal of physical organic chemistry, ISSN 0894-3230, 06/2017, Volume 30, Issue 6
Naphthalene
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2. The chemistry and technology of naphthalene compounds
by Donaldson, Norman
1958, xv, 512 p. illus.
Naphthalene
Book
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3. Full Text Correction: Luminescent imidazolium-naphthalene salts in liquid and solid states
by L'Her, Matthieu and Atoini, Youssef and Fouchet, Julien and Heinrich, Benoît and Del-Giudice, Nicolas and Scrafton, Emma and Bordes, Emilie and Karmazin, Lydia and Charbonnière, Loïc and De Cola, Luisa and Douce, Laurent
New journal of chemistry, ISSN 1144-0546, 2/2020, Volume 44, Issue 6, pp. 2669 - 2669
Naphthalene
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4. Full Text Depurinating naphthalene–DNA adducts in mouse skin related to cancer initiation
by Saeed, Muhammad and Higginbotham, Sheila and Gaikwad, Nilesh and Chakravarti, Dhrubajyoti and Rogan, Eleanor and Cavalieri, Ercole
Free radical biology & medicine, ISSN 0891-5849, 2009, Volume 47, Issue 7, pp. 1075 - 1081
Depurinating naphthalene–DNA adducts | Naphthalene | 1,2-Naphthalene quinone ultimate carcinogenic metabolite | Stable naphthalene–DNA adducts | Metabolic activation of naphthalene | Depurinating naphthalene-DNA adducts | Stable naphthalene-DNA adducts | Biochemistry & Molecular Biology | Endocrinology & Metabolism | Life Sciences & Biomedicine | Science & Technology | Naphthalenes - chemistry | Skin Neoplasms - pathology | Animals | Mice, Inbred SENCAR | DNA Adducts - chemistry | Mice | Naphthalenes - toxicity | Skin Neoplasms - chemically induced | Naphthalenes - metabolism | DNA Adducts - metabolism | Purines | Metabolites | Surface active agents | Analysis | DNA | Quinone | Hydrocarbons | Hormones, Sex | Sulfates | Mass spectrometry | Ethylenediamines | Benzene | Index Medicus
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5. Full Text The Toxicological Effects of Halogenated Naphthalenes: A Review of Aryl Hydrocarbon Receptor-Mediated (Dioxin-like) Relative Potency Factors
by Falandysz, Jerzy and Fernandes, Alwyn and Gregoraszczuk, Ewa and Rose, Martin
Journal of environmental science and health. Part C, Environmental carcinogenesis & ecotoxicology reviews, ISSN 1059-0501, 07/2014, Volume 32, Issue 3, pp. 239 - 272
persistent organic pollutants (POPs) | dioxin-like compounds | mixed brominated/chlorinated naphthalenes | polybrominated naphthalenes | dioxin-like toxicity | polychlorinated naphthalenes | Oncology | Environmental Sciences & Ecology | Toxicology | Life Sciences & Biomedicine | Science & Technology | Environmental Sciences | Naphthalenes - chemistry | Animals | Gas Chromatography-Mass Spectrometry | Rats, Wistar | Rats | Body Burden | Male | Halogens - chemistry | Naphthalenes - pharmacokinetics | Naphthalenes - toxicity | Receptors, Aryl Hydrocarbon - drug effects | Index Medicus
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6. Full Text Synthesis and cycloxygenase inhibitory properties of new naphthalene-methylsulfonamido, naphthalene-methylsulfonyl and tetrahydronaphthalen-methylsulfonamido compounds
by Nencetti, Susanna and Ciccone, Lidia and Rossello, Armando and Nuti, Elisa and Milanese, Claudio and Orlandini, Elisabetta
Journal of enzyme inhibition and medicinal chemistry, ISSN 1475-6366, 05/2015, Volume 30, Issue 3, pp. 406 - 412
naphthalene-methylsulfonamido compounds | Cycloxygenase inhibitors | naphthalene derivatives | tetrahydronaphthalenmethylsulfonamido compounds | naphthalene-methylsulfonyl compounds | Naphthalene-methylsulfonyl compounds | Tetrahydronaphthalenmethylsulfonamido compounds | Naphthalene derivatives | Naphthalene-methylsulfonamido compounds | Pharmacology & Pharmacy | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Chemistry, Medicinal | Science & Technology | Naphthalenes - chemical synthesis | Naphthalenes - chemistry | Sulfonamides - chemistry | Cyclooxygenase Inhibitors - chemistry | Structure-Activity Relationship | Sulfonamides - pharmacology | Cyclooxygenase Inhibitors - pharmacology | Naphthalenes - pharmacology | Dose-Response Relationship, Drug | Sulfonamides - chemical synthesis | Animals | Cyclooxygenase 2 - metabolism | Cyclooxygenase Inhibitors - chemical synthesis | Mice | Molecular Structure | Cyclooxygenase 1 - metabolism | Index Medicus
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7. Full Text Synthesis and photorearrangement of furanone diarylethenes with an additional π-system
by Zakharov, Alexey V and Mitina, Evgenia A and Shirinian, Valerii Z
Tetrahedron letters, ISSN 0040-4039, 08/2020, Volume 61, Issue 34, p. 152277
Furanone | Diarylethene | Photocyclization | Naphthalene | Photorearrangement
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8. Full Text Tuning hydrodearomatization performance of interstitial NixW alloy catalyst by controlling the doping of a small amount of tungsten
by Guan, Qingxin and Yun, Guoxia and Li, Wei
Catalysis today, ISSN 0920-5861, 05/2020
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9. Full Text A non-lithiation route towards facile synthesis of bioactive 4, 9-dimethoxynaphthalide
by Walunj, Raju M and Natu, Arun D and Chikate, Rajeev C and Paradkar, Madhusudan V and Narwade, Santosh C and Kathwate, Gunderao H and Deobagkar, Deepti D
Synthetic communications, ISSN 0039-7911, 10/2020, Volume 50, Issue 20, pp. 3125 - 3132
4,9-dimethoxynaphthalide naphthalene lactone oxidative-cyclization anticancer | Biocompatibility | Naphthalene | Synthesis | Fungicides
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10. Full Text Rationally Designed Surfactants for Few-Layered Graphene Exfoliation: Ionic Groups Attached to Electron-Deficient π‑Conjugated Unit through Alkyl Spacers
by Zhang, Lu and Zhang, Zijian and He, Chaozheng and Dai, Liming and Liu, Jun and Wang, Lixiang
ACS nano, ISSN 1936-0851, 07/2014, Volume 8, Issue 7, pp. 6663 - 6670
naphthalene diimide | ultrasonic exfoliation | dispersion | graphene | surfactant
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11. Full Text Naphthalene derivatives of a conformationally locked GFP chromophore with large stokes shifts
by Baleeva, Nadezhda S and Khavroshechkina, Anastasia V and Zaitseva, Elvira R and Myasnyanko, Ivan N and Zagudaylova, Marina B and Baranov, Mikhail S
Tetrahedron letters, ISSN 0040-4039, 08/2019, Volume 60, Issue 34, p. 150963
Stokes shift | Naphthalene | Fluorophore | Chromophore
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12. Full Text Fluoro‐Substituted n‐Type Conjugated Polymers for Additive‐Free All‐Polymer Bulk Heterojunction Solar Cells with High Power Conversion Efficiency of 6.71
by Jung, Jae Woong and Jo, Jea Woong and Chueh, Chu‐Chen and Liu, Feng and Jo, Won Ho and Russell, Thomas P and Jen, Alex K.‐Y
Advanced materials (Weinheim), ISSN 0935-9648, 06/2015, Volume 27, Issue 21, pp. 3310 - 3317
all‐polymer solar cells | fluorination | naphthalene di‐imide | conjugated polymers | Conjugated polymers | All-polymer solar cells | Fluorination | Naphthalene di-imide | naphthalene di-imide | all-polymer solar cells | Materials Science | Materials Science, Multidisciplinary | Physics, Condensed Matter | Science & Technology - Other Topics | Chemistry, Physical | Physics | Science & Technology | Physics, Applied | Physical Sciences | Chemistry | Nanoscience & Nanotechnology | Technology | Chemistry, Multidisciplinary | Solar cells | Energy use | Polymer industry | Solar batteries | Polymers | Blends | Photocurrent | Photovoltaic cells | Heterojunctions | Charge | Energy conversion efficiency
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13. Full Text The chemical biology of naphthoquinones and its environmental implications
by Kumagai, Yoshito and Shinkai, Yasuhiro and Miura, Takashi and Cho, Arthur K
Annual review of pharmacology and toxicology, ISSN 0362-1642, 2012, Volume 52, Issue 1, pp. 221 - 247
Covalent bond | Oxidative stress | Prooxidant | Redox cycling | Quinone | Electrophile | Biological and medical sciences | Toxicology | General aspects | Environmental pollutants toxicology | Medical sciences | Air Pollutants - analysis | Naphthoquinones - analysis | Quinones - analysis | Reactive Oxygen Species - metabolism | Naphthalenes - analysis | Humans | Carcinogens - analysis | Carcinogens - toxicity | Carcinogens - classification | Anti-Inflammatory Agents - analysis | Cysteine - metabolism | Naphthalenes - chemistry | Quinones - chemistry | Anti-Inflammatory Agents - pharmacology | Cells, Cultured | Naphthoquinones - pharmacology | Environmental Exposure - analysis | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - metabolism | Animals | Anti-Inflammatory Agents - chemistry | Environment | Naphthoquinones - chemistry | Naphthalenes - toxicity | Glyceraldehyde-3-Phosphate Dehydrogenases - metabolism | Air Pollutants - chemistry | Environmental aspects | Environmental chemistry | Chemical properties | Research | Environmental impact analysis | Index Medicus | Enzymes | Oxygen | Toxicity | Lung diseases | Vapors | Aromatic hydrocarbons | Particulates | Combustion | Inflammation | regulatory proteins | Fuels | Proteins | Signal transduction | natural products | Tobacco | Naphthalene | Reviews | Metabolites | Glycolysis | Air pollution | Glyceraldehyde-3-phosphate dehydrogenase | Protein-tyrosine-phosphatase
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14. Full Text Strategies for the Synthesis of Functional Naphthalene Diimides
by Suraru, Sabin‐Lucian and Würthner, Frank
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2014, Volume 53, Issue 29, pp. 7428 - 7448
dyes/pigments | organic semiconductors | annulation | naphthalene diimides | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Semiconductors | Electronic properties | Naphthalene | Accessibility | Electronics | Strategy | N-type semiconductors | Derivatives | Adjustable | Diimide
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