Статті в журналах з теми "Derivative of o-aminobenzoic acids"
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Zhao, MJ, D. Robert та L. Jung. "New agents for cutaneous photoprotection: derivatives of α-amino acids, 4-aminobenzoic and 4-methoxycinnamic acids". European Journal of Medicinal Chemistry 28, № 12 (січень 1993): 949–54. http://dx.doi.org/10.1016/0223-5234(93)90050-o.
Повний текст джерелаDuggan, BM, RL Laslett, and JFK Wilshire. "Studies in Thiohydantoin Chemistry. I. Some Aspects of the Schlack-Kumpf Reaction." Australian Journal of Chemistry 49, no. 5 (1996): 541. http://dx.doi.org/10.1071/ch9960541.
Повний текст джерелаSlavíková, Tereza, Vladimír Pouzar та Ivan Černý. "Synthesis of Steroid O-(ω-Hydroxyalkyl)oximes by Reduction of Corresponding O-(ω-Carboxyalkyl)oxime Derivatives". Collection of Czechoslovak Chemical Communications 63, № 4 (1998): 557–76. http://dx.doi.org/10.1135/cccc19980557.
Повний текст джерелаÇalış, Ihsan, S. Serap Birincioǧlu, Hasan Kırmızıbekmez, Bernhard Pfeiffer, and Jörg Heilmann. "Secondary Metabolites from Asphodelus aestivus." Zeitschrift für Naturforschung B 61, no. 10 (October 1, 2006): 1304–10. http://dx.doi.org/10.1515/znb-2006-1019.
Повний текст джерелаFreire, C. S. R., A. J. D. Silvestre, and C. Pascoal Neto. "Oxidized Derivatives of Lipophilic Extractives Formed during Hardwood Kraft Pulp Bleaching." Holzforschung 57, no. 5 (August 20, 2003): 503–12. http://dx.doi.org/10.1515/hf.2003.075.
Повний текст джерелаSpassova, Maria K., Antonín Holý, and Milena Masojídková. "Ribonucleosides of 3-amino- and 3,5-diaminopyrazole-4-carboxylic acid and their open-chain analogues: Synthesis and reactions." Collection of Czechoslovak Chemical Communications 51, no. 7 (1986): 1512–31. http://dx.doi.org/10.1135/cccc19861512.
Повний текст джерелаSpitaler, Renate, Ernst-P. Ellmerer, Christian Zidorn, and Hermann Stuppner. "A New Eudesmane Derivative from Leontodon tuberosus." Zeitschrift für Naturforschung B 59, no. 1 (January 1, 2004): 95–99. http://dx.doi.org/10.1515/znb-2004-0113.
Повний текст джерелаLandaeta Aponte, Roselis A., Andreas Luxenburger, Scott A. Cameron, Alex Weymouth-Wilson, Richard H. Furneaux, Lawrence D. Harris, and Benjamin J. Compton. "Synthesis of Novel C/D Ring Modified Bile Acids." Molecules 27, no. 7 (April 6, 2022): 2364. http://dx.doi.org/10.3390/molecules27072364.
Повний текст джерелаGuimarães, Anderson C., Alvicler Magalhães, Marcos J. Nakamura, Antonio C. Siani, Christina Barja-Fidalgo, and André L. F. Sampaio. "Flavonoids Bearing an O-Arabinofuranosyl-(1→3)-Rhamnoside Moiety from Cladocolea Micrantha: Inhibitory Effect on Human Melanoma Cells." Natural Product Communications 7, no. 10 (October 2012): 1934578X1200701. http://dx.doi.org/10.1177/1934578x1200701014.
Повний текст джерелаQi, Xiao Yan, Lin Wu, Jian Guo Wang, and De Lian Yi. "A Novel Synthesis of Acetophenone Benzopyran Derivative." Advanced Materials Research 152-153 (October 2010): 1483–86. http://dx.doi.org/10.4028/www.scientific.net/amr.152-153.1483.
Повний текст джерелаNguyen, Thi Thu Huong, Jiří Urban, Eva Klinotová, Jan Sejbal, Jiří Protiva, Pavel Drašar, and Miroslav Protiva. "Synthesis of Several Hydroxylated 23-(Benzimidazol-2-yl-, Benzoxazol-2-yl and Benzothiazol-2-yl)norcholanes and Some Related Compounds." Collection of Czechoslovak Chemical Communications 60, no. 2 (1995): 257–75. http://dx.doi.org/10.1135/cccc19950257.
Повний текст джерелаBegum, Parvin, Yasuyuki Hashidoko, Md Tofazzal Islam, Yuko Ogawa, and Satoshi Tahara. "Zoosporicidal Activities of Anacardic Acids against Aphanomyces cochlioides." Zeitschrift für Naturforschung C 57, no. 9-10 (October 1, 2002): 874–82. http://dx.doi.org/10.1515/znc-2002-9-1020.
Повний текст джерелаWanjala, George W., Arnold N. Onyango, David Abuga, Calvin Onyango, and Moses Makayoto. "Evidence for the Formation of Ozone (or Ozone-Like Oxidants) by the Reaction of Singlet Oxygen with Amino Acids." Journal of Chemistry 2018 (September 13, 2018): 1–6. http://dx.doi.org/10.1155/2018/6145180.
Повний текст джерелаDrzazga, Anna, Marta Okulus, Magdalena Rychlicka, Łukasz Biegała, Anna Gliszczyńska, and Edyta Gendaszewska-Darmach. "Lysophosphatidylcholine Containing Anisic Acid Is Able to Stimulate Insulin Secretion Targeting G Protein Coupled Receptors." Nutrients 12, no. 4 (April 22, 2020): 1173. http://dx.doi.org/10.3390/nu12041173.
Повний текст джерелаZhu, Min Peng, Su Hong Li, Xiu Hong Zhao, and Peng Guan. "Sample Preparation for HPLC Determination of Free and Oligosaccharides-Bound Sialic Acid in Bovine Colostrum." Advanced Materials Research 641-642 (January 2013): 882–85. http://dx.doi.org/10.4028/www.scientific.net/amr.641-642.882.
Повний текст джерелаSkała, Ewa, Agnieszka Kicel, Monika A. Olszewska, Anna K. Kiss, and Halina Wysokińska. "Establishment of Hairy Root Cultures ofRhaponticum carthamoides(Willd.) Iljin for the Production of Biomass and Caffeic Acid Derivatives." BioMed Research International 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/181098.
Повний текст джерелаKefurt, Karel, Zdeňka Kefurtová, and Jiří Jarý. "6-Amino-6-deoxyhexonolactams." Collection of Czechoslovak Chemical Communications 53, no. 8 (1988): 1795–805. http://dx.doi.org/10.1135/cccc19881795.
Повний текст джерелаSmith, Graham, and Urs D. Wermuth. "Hydrogen bonding in cyclic imides and amide carboxylic acid derivatives from the facile reaction ofcis-cyclohexane-1,2-carboxylic anhydride witho- andp-anisidine andm- andp-aminobenzoic acids." Acta Crystallographica Section C Crystal Structure Communications 68, no. 9 (August 1, 2012): o327—o331. http://dx.doi.org/10.1107/s0108270112030168.
Повний текст джерелаKantlehner, Willi, Rüdiger Stieglitz, Hansjörg Lehmann, and Markus Vettel. "Orthoamide und Iminiumsalze, IIIC. Weitere Ergebnisse bei der Umsetzung von Orthoamiden der Alkincarbonsäuren mit CH2- und CH2/NH-aciden Verbindungen." Zeitschrift für Naturforschung B 74, no. 11-12 (December 18, 2019): 925–38. http://dx.doi.org/10.1515/znb-2019-0078.
Повний текст джерелаHellebø, Audny, Ulrike Vilas, Knut Falk, and Reinhard Vlasak. "Infectious Salmon Anemia Virus Specifically Binds to and Hydrolyzes 4-O-Acetylated Sialic Acids." Journal of Virology 78, no. 6 (March 15, 2004): 3055–62. http://dx.doi.org/10.1128/jvi.78.6.3055-3062.2004.
Повний текст джерелаTandon, Manju, Piyush Kumar, Haiyan Xia, Lili Wang та Leonard I. Wiebe. "Synthesis of Bromophenyl β-D-Glucuronides: Hydrophilic Precursors of Lipophilic Standards in the Analysis of Environmental Polychlorinated Biphenyls". Collection of Czechoslovak Chemical Communications 71, № 7 (2006): 1042–50. http://dx.doi.org/10.1135/cccc20061042.
Повний текст джерелаGao, Rui Han, Ying Fan, Bo Xiao, Peng Chen, Jian Xin Zhang, Qing-di Zhou, Sai Feng Xue, Qian Jiang Zhu, and Zhu Tao. "Direct syntheses of cucurbit[7]uril-anchored polyacrylic acid microspheres and adsorption of basic dyes by the derivative." RSC Advances 5, no. 81 (2015): 65775–79. http://dx.doi.org/10.1039/c5ra09064d.
Повний текст джерелаShaw, W., E. Kassen, and E. Chaves. "Increased urinary excretion of analogs of Krebs cycle metabolites and arabinose in two brothers with autistic features." Clinical Chemistry 41, no. 8 (August 1, 1995): 1094–104. http://dx.doi.org/10.1093/clinchem/41.8.1094.
Повний текст джерелаKliegel, Wolfgang, Ute Schumacher, Steven J. Rettig, and James Trotter. "Structural studies of organoboron compounds LXIV. Boron chelate formation with glycolohydroxamic acids, and the crystal and molecular structure of 5-(1-hydroxycyclohexyl)-2,2-diphenyl-1,3-dioxa-4-azonia-2-borata-4-cyclopentane." Canadian Journal of Chemistry 74, no. 3 (March 1, 1996): 445–52. http://dx.doi.org/10.1139/v96-048.
Повний текст джерелаMurata, Toshihiro, Tatsuo Katagiri, Masaaki Osaka, Shohei Yamauchi, Kenshi Yoshimura, Manami Kawada, Yu Fujii, Yuka Suzuki, and Kenroh Sasaki. "Hyaluronidase and degranulation inhibitors from the edible roots of Oenanthe javanica including seric acids F and G that were obtained by heating." Bioscience, Biotechnology, and Biochemistry 85, no. 2 (January 20, 2021): 369–77. http://dx.doi.org/10.1093/bbb/zbaa042.
Повний текст джерелаSlobodianiuk, Oksana, Oleksandra Berezhnytska, Tetyana Kamens'ka, and Мария Русакова. "SYNTHESIS AND PROPERTIES OF NEW N-ACYL DERIVATIVES OF ANTHRANILIC ACID." Ukrainian Chemistry Journal 85, no. 4 (June 7, 2019): 59–70. http://dx.doi.org/10.33609/0041-6045.85.4.2019.59-70.
Повний текст джерелаGazotti, W. A., R. Faez, and Marco-A. De Paoli. "Electrochemical, electrochromic and photoelectrochemical behavior of a highly soluble polyaniline derivative: poly(o-methoxyaniline) doped with functionalized organic acids." Journal of Electroanalytical Chemistry 415, no. 1-2 (October 1996): 107–13. http://dx.doi.org/10.1016/s0022-0728(96)04712-2.
Повний текст джерелаPolívka, Zdeněk, Miloš Buděšínský, Jiří Holubek, Bohdan Schneider, Zdeněk Šedivý, Emil Svátek, Oluše Matoušová, et al. "4H-Benzo[4,5]cyclohepta[1,2-b]thiophenes and 9,10-dihydro derivatives - Sulfonium analogues of pizotifen and ketotifen; Chirality of ketotifen; Synthesis of the 2-bromo derivative of ketotifen." Collection of Czechoslovak Chemical Communications 54, no. 9 (1989): 2443–69. http://dx.doi.org/10.1135/cccc19892443.
Повний текст джерелаSatsuma, Koji, Minoru Masuda, and Kiyoshi Sato. "O-Demethylation and Successive Oxidative Dechlorination of Methoxychlor by Bradyrhizobium sp. Strain 17-4, Isolated from River Sediment." Applied and Environmental Microbiology 78, no. 15 (May 25, 2012): 5313–19. http://dx.doi.org/10.1128/aem.01180-12.
Повний текст джерелаModro, Agnes M., and Tomasz A. Modro. "The prototropic equilibria in pentenylphosphonic systems." Canadian Journal of Chemistry 66, no. 7 (July 1, 1988): 1541–45. http://dx.doi.org/10.1139/v88-250.
Повний текст джерелаHimbert, Gerhard, and Dieter Fink. "Cycloadditionen, XXII [1]. Synthese und thermische Reaktion von S-(Alkyl/Aryl)- 2.3-butadienthiosäure-estern / Cycloadditions, XXII [1]. Synthesis and Thermal Reaction of S-(Alkyl/Aryl)-2,3-butadienethioates." Zeitschrift für Naturforschung B 49, no. 4 (April 1, 1994): 542–50. http://dx.doi.org/10.1515/znb-1994-0417.
Повний текст джерелаJaneba, Zlatko, Milena Masojídková, and Antonín Holý. "Alternative synthesis of 9-{3-[(diisopropoxyphosphoryl)methoxy]-2-hydroxypropyl}adenine and its free phosphonates substituted at the C-8 position of purine base." Collection of Czechoslovak Chemical Communications 75, no. 3 (2010): 371–81. http://dx.doi.org/10.1135/cccc2009569.
Повний текст джерелаGómez-López, Iván, Gloria Lobo-Rodrigo, María P. Portillo, and M. Pilar Cano. "Characterization, Stability, and Bioaccessibility of Betalain and Phenolic Compounds from Opuntia stricta var. Dillenii Fruits and Products of Their Industrialization." Foods 10, no. 7 (July 9, 2021): 1593. http://dx.doi.org/10.3390/foods10071593.
Повний текст джерелаBarbero, Margherita, Silvano Cadamuro, Stefano Dughera, and Giovanni Ghigo. "o-Benzenedisulfonimide and its chiral derivative as Brønsted acids catalysts for one-pot three-component Strecker reaction. Synthetic and mechanistic aspects." Organic & Biomolecular Chemistry 10, no. 20 (2012): 4058. http://dx.doi.org/10.1039/c2ob25584g.
Повний текст джерелаPacheco, Juan M., Tina M. Henry, Vivian K. O'Donnell, Jason B. Gregory, and Peter W. Mason. "Role of Nonstructural Proteins 3A and 3B in Host Rangeand Pathogenicity of Foot-and-Mouth DiseaseVirus." Journal of Virology 77, no. 24 (December 15, 2003): 13017–27. http://dx.doi.org/10.1128/jvi.77.24.13017-13027.2003.
Повний текст джерелаWatt, Jacinta A., Carlie T. Gannon, Karen J. Loft, Zoran Dinev, and Spencer J. Williams. "'Click' Preparation of Carbohydrate 1-Benzotriazoles, 1,4-Disubstituted, and 1,4,5-Trisubstituted Triazoles and their Utility as Glycosyl Donors." Australian Journal of Chemistry 61, no. 11 (2008): 837. http://dx.doi.org/10.1071/ch08364.
Повний текст джерелаTomori, Hiroshi, Hisayoshi Yoshihara, and Katsuyuki Ogura. "Facile Optical Resolution of a Dibenzopyrazinoazepine Derivative and the Nature of Molecular Recognition of Amines by Chiral 2,3-Di-O-(arylcarbonyl)tartaric Acids." Bulletin of the Chemical Society of Japan 69, no. 12 (December 1996): 3581–90. http://dx.doi.org/10.1246/bcsj.69.3581.
Повний текст джерелаBarbero, Margherita, Silvano Cadamuro, Stefano Dughera, and Giovanni Ghigo. "ChemInform Abstract: o-Benzenedisulfonimide and Its Chiral Derivative as Broensted Acids Catalysts for One-Pot Three-Component Strecker Reaction. Synthetic and Mechanistic Aspects." ChemInform 43, no. 43 (September 27, 2012): no. http://dx.doi.org/10.1002/chin.201243071.
Повний текст джерелаLopez-Anaya, A., and M. Mayersohn. "Ascorbic and dehydroascorbic acids simultaneously quantified in biological fluids by liquid chromatography with fluorescence detection, and comparison with a colorimetric assay." Clinical Chemistry 33, no. 10 (October 1, 1987): 1874–78. http://dx.doi.org/10.1093/clinchem/33.10.1874.
Повний текст джерелаBirzoi, Roxana M., Delia Bugnariu, Christine Goers, Rafael Guerrero Gimeno, Thorsten Gust, Antje Riecke, Zoltán Benkõ, et al. "Di(phosphavinyl) Ethers (2,4-Diphospha-3-oxapentadienes)." Zeitschrift für Naturforschung B 64, no. 1 (January 1, 2009): 73–82. http://dx.doi.org/10.1515/znb-2009-0110.
Повний текст джерелаFási, Laura, Ahmed Dhahir Latif, István Zupkó, Sándor Lévai, Miklós Dékány, Zoltán Béni, Árpád Könczöl, György Tibor Balogh, and Attila Hunyadi. "AAPH or Peroxynitrite-Induced Biorelevant Oxidation of Methyl Caffeate Yields a Potent Antitumor Metabolite." Biomolecules 10, no. 11 (November 11, 2020): 1537. http://dx.doi.org/10.3390/biom10111537.
Повний текст джерелаTraisaeng, Supitchaya, Deron Raymond Herr, Hsin-Jou Kao, Tsung-Hsien Chuang, and Chun-Ming Huang. "A Derivative of Butyric Acid, the Fermentation Metabolite of Staphylococcus epidermidis, Inhibits the Growth of a Staphylococcus aureus Strain Isolated from Atopic Dermatitis Patients." Toxins 11, no. 6 (May 31, 2019): 311. http://dx.doi.org/10.3390/toxins11060311.
Повний текст джерелаChen, Buze, Sicong Liu, Haihong Wang, Guilin Li, Xiaoyuan Lu, and Hao Xu. "Differential Expression Profiles and Function Prediction of Transfer RNA-Derived Fragments in High-Grade Serous Ovarian Cancer." BioMed Research International 2021 (March 30, 2021): 1–17. http://dx.doi.org/10.1155/2021/5594081.
Повний текст джерелаHarmrolfs, Kirsten, Lena Mancuso, Binia Drung, Florenz Sasse, and Andreas Kirschning. "Preparation of new alkyne-modified ansamitocins by mutasynthesis." Beilstein Journal of Organic Chemistry 10 (March 3, 2014): 535–43. http://dx.doi.org/10.3762/bjoc.10.49.
Повний текст джерелаArgentieri, Maria Pia, Moira Madeo, Pinarosa Avato, Marcello Iriti, and Sara Vitalini. "Polyphenol content and bioactivity of Achillea moschata from the Italian and Swiss Alps." Zeitschrift für Naturforschung C 75, no. 3-4 (March 26, 2020): 57–64. http://dx.doi.org/10.1515/znc-2019-0214.
Повний текст джерелаMseer, Marwa Abdulameer, Khudheyer Jawad, and Yahya Al-Khafaji. "Synthesis and Characterization of Heterocyclic Compounds Derived from Schiff base Glycerol Triester." NeuroQuantology 19, no. 9 (October 12, 2021): 88–96. http://dx.doi.org/10.14704/nq.2021.19.9.nq21141.
Повний текст джерелаDragović, Sanja, Verica Dragović-Uzelac, Sandra Pedisić, Zrinka Čošić, Maja Friščić, Ivona Elez Garofulić, and Zoran Zorić. "The Mastic Tree (Pistacia lentiscus L.) Leaves as Source of BACs: Effect of Growing Location, Phenological Stage and Extraction Solvent on Phenolic Content." Food Technology and Biotechnology 58, no. 3 (July 15, 2020): 303–13. http://dx.doi.org/10.17113/ftb.58.03.20.6662.
Повний текст джерелаUdvardy, Antal, Csenge Tamara Szolnoki, Réka Gombos, Gábor Papp, Éva Kováts, Ferenc Joó, and Ágnes Kathó. "Mechanochemical P-derivatization of 1,3,5-Triaza-7-Phosphaadamantane (PTA) and Silver-Based Coordination Polymers Obtained from the Resulting Phosphabetaines." Molecules 25, no. 22 (November 16, 2020): 5352. http://dx.doi.org/10.3390/molecules25225352.
Повний текст джерелаBvenura, Callistus, and Learnmore Kambizi. "Composition of Phenolic Compounds in South African Schinus molle L. Berries." Foods 11, no. 10 (May 10, 2022): 1376. http://dx.doi.org/10.3390/foods11101376.
Повний текст джерелаLehrer, Jason, Karen A. Vigeant, Laura D. Tatar, and Miguel A. Valvano. "Functional Characterization and Membrane Topology of Escherichia coli WecA, a Sugar-Phosphate Transferase Initiating the Biosynthesis of Enterobacterial Common Antigen and O-Antigen Lipopolysaccharide." Journal of Bacteriology 189, no. 7 (January 19, 2007): 2618–28. http://dx.doi.org/10.1128/jb.01905-06.
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