Статті в журналах з теми "Stereoisomeri"
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Costa, Maria L. M., Miguel Borges, Evaldo F. Vilela, Paulo de Marco Jr, and Eraldo R. Lima. "Effect of stereoisomers of the main component of the sex pheromone of Euschistus heros (F.) (Hemiptera: Pentatomidae) in the attractiveness of females." Anais da Sociedade Entomológica do Brasil 29, no. 3 (September 2000): 413–22. http://dx.doi.org/10.1590/s0301-80592000000300004.
Повний текст джерелаLapčík, Oldřich, Richard Hampl, Martin Hill, Luboslav Stárka, Alexander Kasal, Vladimír Pouzar, and Zdeněk Putz. "Radioimmunological and Chromatographic Properties of Tyrosine Methyl Ester Conjugates with Stereoisomeric Steroid Carboxy Derivatives." Collection of Czechoslovak Chemical Communications 61, no. 5 (1996): 799–807. http://dx.doi.org/10.1135/cccc19960799.
Повний текст джерелаKuchan, Matthew J., Søren K. Jensen, Elizabeth J. Johnson та Jacqueline C. Lieblein-Boff. "The naturally occurring α-tocopherol stereoisomer RRR-α-tocopherol is predominant in the human infant brain". British Journal of Nutrition 116, № 1 (16 травня 2016): 126–31. http://dx.doi.org/10.1017/s0007114516001719.
Повний текст джерелаSheikh, Ishfaq Ahmad, and Mohd Amin Beg. "Structural Aspects of Potential Endocrine-Disrupting Activity of Stereoisomers for a Common Pesticide Permethrin against Androgen Receptor." Biology 10, no. 2 (February 11, 2021): 143. http://dx.doi.org/10.3390/biology10020143.
Повний текст джерелаDIEUAIDE-NOUBHANI, Martine, Stanny ASSELBERGHS, Guy P. MANNAERTS та Paul P. VAN VELDHOVEN. "Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal β-oxidation of pristanic acid". Biochemical Journal 325, № 2 (15 липня 1997): 367–73. http://dx.doi.org/10.1042/bj3250367.
Повний текст джерелаDersjant-Li, Jensen, Bos та Peisker. "Bio-discrimination of α-tocopherol Stereoisomers in Rearing and Veal Calves Fed Milk Replacer Supplemented with All-rac-α-tocopheryl Acetate". International Journal for Vitamin and Nutrition Research 79, № 4 (1 липня 2009): 199–211. http://dx.doi.org/10.1024/0300-9831.79.4.199.
Повний текст джерелаTirri, Micaela, Paolo Frisoni, Sabrine Bilel, Raffaella Arfè, Claudio Trapella, Anna Fantinati, Giorgia Corli, et al. "Worsening of the Toxic Effects of (±)Cis-4,4′-DMAR Following Its Co-Administration with (±)Trans-4,4′-DMAR: Neuro-Behavioural, Physiological, Immunohistochemical and Metabolic Studies in Mice." International Journal of Molecular Sciences 22, no. 16 (August 16, 2021): 8771. http://dx.doi.org/10.3390/ijms22168771.
Повний текст джерелаCortinas, Lucia, Ana Barroeta, Jaume Galobart та Søren K. Jensen. "Distribution of α-tocopherol stereoisomers in liver and thigh of chickens". British Journal of Nutrition 92, № 2 (серпень 2004): 295–301. http://dx.doi.org/10.1079/bjn20041188.
Повний текст джерелаHymøller, Lone, Saman Lashkari, Tove N. Clausen та Søren K. Jensen. "Distribution of α-tocopherol stereoisomers in mink (Mustela vison) organs varies with the amount of all-rac-α-tocopheryl acetate in the diet". British Journal of Nutrition 120, № 12 (17 жовтня 2018): 1332–37. http://dx.doi.org/10.1017/s0007114518002878.
Повний текст джерелаBrice-Tutt, Ariana C., Sanjeewa N. Senadheera, Michelle L. Ganno, Shainnel O. Eans, Tanvir Khaliq, Thomas F. Murray, Jay P. McLaughlin, and Jane V. Aldrich. "Phenylalanine Stereoisomers of CJ-15,208 and [d-Trp]CJ-15,208 Exhibit Distinctly Different Opioid Activity Profiles." Molecules 25, no. 17 (September 2, 2020): 3999. http://dx.doi.org/10.3390/molecules25173999.
Повний текст джерелаLicea Perez, Hermes, and Clara Andonian. "Chemical derivatization in combination with supercritical fluid chromatography to improve resolution of stereoisomers." Bioanalysis 13, no. 12 (June 2021): 985–99. http://dx.doi.org/10.4155/bio-2021-0053.
Повний текст джерелаPerlikowska, Wiesława, Remigiusz Żurawiński, and Marian Mikołajczyk. "A new and expeditious synthesis of all enantiomerically pure stereoisomers of rosaprostol, an antiulcer drug." Beilstein Journal of Organic Chemistry 12 (October 21, 2016): 2234–39. http://dx.doi.org/10.3762/bjoc.12.215.
Повний текст джерелаPresini, Francesco, Graziano Di Carmine, Pier Paolo Giovannini, Virginia Cristofori, Lindomar Alberto Lerin, Olga Bortolini, Claudio Trapella, and Anna Fantinati. "Chemoenzymatic Stereodivergent Synthesis of All the Possible Stereoisomers of the 2,3-Dimethylglyceric Acid Ethyl Ester." Catalysts 11, no. 12 (November 26, 2021): 1440. http://dx.doi.org/10.3390/catal11121440.
Повний текст джерелаJia, Qi, Nana Xu, Pengqian Mu, Bo Wang, Shuming Yang, and Jing Qiu. "Stereoselective Separation and Acute Toxicity of Tau-Fluvalinate to Zebrafish." Journal of Chemistry 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/931908.
Повний текст джерелаMcIntosh, John M., and Ivy E. E. Hayes. "Stereochemistry of 3-carboxylated 2,5-dihydrothiophene formation." Canadian Journal of Chemistry 65, no. 1 (January 1, 1987): 110–13. http://dx.doi.org/10.1139/v87-018.
Повний текст джерелаDuong-Thi, Minh-Dao, Maria Bergström, Tomas Fex, Susanne Svensson, Sten Ohlson, and Roland Isaksson. "Weak Affinity Chromatography for Evaluation of Stereoisomers in Early Drug Discovery." Journal of Biomolecular Screening 18, no. 6 (March 11, 2013): 748–55. http://dx.doi.org/10.1177/1087057113480391.
Повний текст джерелаPham, Hoai, Madelyn Hunsley, Chou-Hsun Yang, Haobin Wang, and Scott M. Reed. "Demonstration of a Stereospecific Photochemical Meta Effect." Photochem 2, no. 1 (January 12, 2022): 69–76. http://dx.doi.org/10.3390/photochem2010006.
Повний текст джерелаCastillo-Aguirre, Alver A., Zuly Jenny Rivera Monroy, and Mauricio Maldonado. "Analysis by RP-HPLC and Purification by RP-SPE of the C-Tetra(p-hydroxyphenyl)resorcinolarene Crown and Chair Stereoisomers." Journal of Analytical Methods in Chemistry 2019 (April 16, 2019): 1–6. http://dx.doi.org/10.1155/2019/2051282.
Повний текст джерелаLandge, Shashikant B., Sanjay A. Jadhav, Sunil B. Dahale, Navanath C. Niphade, Ch Lakshmi Narayana, Vishwas B. Gaikwad, and Vijayavitthal T. Mathad. "Development and Validation of New Chromatographic Method for the Determination of Enantiomeric and Diastereomeric Purity of Solifenacin Succinate: An Antimuscarinic Agent." Chromatography Research International 2011 (October 21, 2011): 1–7. http://dx.doi.org/10.4061/2011/243491.
Повний текст джерелаTonoi, Takayuki, Takehiko Inohana, Teruyuki Sato, Yuuki Noda, Miyuki Ikeda, Miku Akutsu, Takatsugu Murata, et al. "Total Synthesis and Antimicrobial Evaluation of 23-Demethyleushearilide and Extensive Antimicrobial Evaluation of All Synthetic Stereoisomers of (16Z,20E)-Eushearilide and (16E,20E)-Eushearilide." Molecules 24, no. 19 (September 22, 2019): 3437. http://dx.doi.org/10.3390/molecules24193437.
Повний текст джерелаRousselin, Yoann, Hugo Laureano, and Alexandre Clavel. "Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman." Acta Crystallographica Section E Crystallographic Communications 71, no. 8 (July 8, 2015): o552—o553. http://dx.doi.org/10.1107/s205698901501261x.
Повний текст джерелаKuchan, Matthew J., Katherine M. Ranard, Priyankar Dey, Sookyoung Jeon, Geoff Y. Sasaki, Karen J. Schimpf, Richard S. Bruno, Martha Neuringer та John W. Erdman. "Infant Rhesus Macaque Brain α-Tocopherol Stereoisomer Profile Is Differentially Impacted by the Source of α-Tocopherol in Infant Formula". Journal of Nutrition 150, № 9 (2 липня 2020): 2305–13. http://dx.doi.org/10.1093/jn/nxaa174.
Повний текст джерелаFUJITA, Shinsaku. "RS-Stereoisomeric Groups and Enumeration of Quadruplets of RS-Stereoisomers." Journal of Computer Chemistry, Japan 13, no. 3 (2014): 155–56. http://dx.doi.org/10.2477/jccj.2014-0014.
Повний текст джерелаIl`in, E. G., A. S. Parshakov, V. G. Yarzhemsky, E. A. Ugolkova, L. V. Goyeva, and V. I. Privalov. "Physical chemistry CeF4 complexes in organic solvents." Доклады Академии наук 488, no. 1 (September 24, 2019): 47–51. http://dx.doi.org/10.31857/s0869-5652488147-51.
Повний текст джерелаBencke, Carlos, Mário Marangoni, Adriano Camargo, Cassio Fantinel, Helio Bonacorso, Marcos Martins, and Nilo Zanatta. "Synthesis of Penta-2,4-dienenitriles by the Horner–Wadsworth–Emmons Olefination of Enones." Synthesis 49, no. 23 (August 24, 2017): 5131–42. http://dx.doi.org/10.1055/s-0036-1590871.
Повний текст джерелаKIDANE, A., I. L. NESHEIM, H. J. S. LARSEN, E. THUEN, S. K. JENSEN та H. STEINSHAMN. "Effects of supplementing mid-lactation dairy cows with seaweed and vitamin E on plasma and milk α-tocopherol and antibody response to immunization". Journal of Agricultural Science 153, № 5 (18 березня 2015): 929–42. http://dx.doi.org/10.1017/s0021859615000052.
Повний текст джерелаAnderbrant, Olle, D. Barry Lyons, Joakim Bång, Erik Hedenström, and Hans-Erik Högberg. "Sex Pheromone of the Introduced Pine Sawfly, Diprion similis, Revisited to Define a Useful Monitoring Lure: Deviating Chiral Composition and Behavioural Responses Compared to Earlier Reports." Insects 12, no. 10 (September 29, 2021): 886. http://dx.doi.org/10.3390/insects12100886.
Повний текст джерелаFujita, Shinsaku. "Klein Four-Group as the Factor Group for Elucidating RS-Stereoisomerism of Cubane Derivatives. The Factor-Group Method for Type-Itemized Enumeration of Stereoisograms." MATCH Communications in Mathematical and in Computer Chemistry 88, no. 2 (2022): 239–318. http://dx.doi.org/10.46793/match.88-2.239f.
Повний текст джерелаXu, Yangrong, Hangjun Tang, Yijie Xu, Jialin Guo, Xu Zhao, Qingguo Meng та Junhai Xiao. "Design, Synthesis, Bioactivity Evaluation, Crystal Structures, and In Silico Studies of New α-Amino Amide Derivatives as Potential Histone Deacetylase 6 Inhibitors". Molecules 27, № 10 (22 травня 2022): 3335. http://dx.doi.org/10.3390/molecules27103335.
Повний текст джерелаLeitgeb, Balázs. "Spatial relationships between the pharmacophores of endomorphin-2: a comparative study of stereoisomers." Open Chemistry 10, no. 6 (December 1, 2012): 1791–98. http://dx.doi.org/10.2478/s11532-012-0105-3.
Повний текст джерелаBernát, Juraj, Ladislav Kniežo, Gabriela Birošová, Miloš Buděšínský, Jaroslav Podlaha, Jana Podlahová, and Jiří Novotný. "Reactions of PO(NCS)3 with 4-Hydroxy-1,3-dioxanes. Crystal Structure of rel-(2S,4R,5S,6S)-2,6-Diethyl-5-methyl-4-(N'-benzylthioureido)-1,3-dioxane." Collection of Czechoslovak Chemical Communications 57, no. 6 (1992): 1299–313. http://dx.doi.org/10.1135/cccc19921299.
Повний текст джерелаBrine, G. A., F. I. Carroll, T. M. Richardson-Leibert, H. Xu, and R. B. Rothman. "Ohmefentanyl and Its Stereoisomers: Chemistry and Pharmacology." Current Medicinal Chemistry 4, no. 4 (August 1997): 247–70. http://dx.doi.org/10.2174/0929867304666220313115017.
Повний текст джерелаOzenil, Marius, Jonas Aronow, Daniela Piljak, Chrysoula Vraka, Wolfgang Holzer, Helmut Spreitzer, Wolfgang Wadsak, Marcus Hacker, and Verena Pichler. "Synthesis, Biological, and Computational Evaluation of Antagonistic, Chiral Hydrobenzoin Esters of Arecaidine Targeting mAChR M1." Pharmaceuticals 13, no. 12 (November 30, 2020): 437. http://dx.doi.org/10.3390/ph13120437.
Повний текст джерелаJežek, Rudolf, Miroslava Žertová, Jiřina Slaninová, Pavel Majer, and Zdenko Procházka. "Antagonistic Analogs of Oxytocin with Substituted Phenylalanine or Tyrosine in Position 2." Collection of Czechoslovak Chemical Communications 59, no. 6 (1994): 1430–38. http://dx.doi.org/10.1135/cccc19941430.
Повний текст джерелаPolívka, Zdeněk, Jiří Holubek, Emil Svátek, Jan Metyš, and Miroslav Protiva. "Synthesis of the semi-rigid analogues of prothiadene and dithiadene as potential antidepressant and antihistamine agents: 11-[2-(Dimethylaminomethyl)cyclohexylidene]-6,11-dihydrodibenzo[b,e]thiepins and 4-[2-(dimethylaminomethyl)cyclohexylidene]-4,9-dihydrothieno-[2,3-c]-2-benzothiepins." Collection of Czechoslovak Chemical Communications 50, no. 5 (1985): 1078–88. http://dx.doi.org/10.1135/cccc19851078.
Повний текст джерелаGill, Brendon D., Jackie E. Wood та Harvey E. Indyk. "Analysis of α-Tocopherol Stereoisomers in Fortified Infant Formula by Chiral Chromatography". Journal of AOAC INTERNATIONAL 104, № 3 (23 січня 2021): 725–31. http://dx.doi.org/10.1093/jaoacint/qsab012.
Повний текст джерелаHenthorn, Thomas K., Tom C. Krejcie, Claus U. Niemann, Cheri Enders-Klein, Colin A. Shanks, and Michael J. Avram. "Ketamine Distribution Described by a Recirculatory Pharmacokinetic Model Is Not Stereoselective." Anesthesiology 91, no. 6 (December 1, 1999): 1733. http://dx.doi.org/10.1097/00000542-199912000-00027.
Повний текст джерелаReichert, Sylvia, Matthias Wüst, Thomas Beck, and Armin Mosandl. "Stereoisomeric Flavor Compounds LXXXI: Dill Ether and Itscis-Stereoisomers: Synthesis and Enantioselective Analysis." Journal of High Resolution Chromatography 21, no. 3 (March 1, 1998): 185–88. http://dx.doi.org/10.1002/(sici)1521-4168(19980301)21:3<185::aid-jhrc185>3.0.co;2-j.
Повний текст джерелаReichert, Sylvia, and Armin Mosandl. "Stereoisomeric Flavor Compounds LXXXII Dill Ether and Its Stereoisomers: Synthesis and Enantioselective Analysis." Journal of High Resolution Chromatography 22, no. 11 (November 1, 1999): 631–34. http://dx.doi.org/10.1002/(sici)1521-4168(19991101)22:11<631::aid-jhrc631>3.0.co;2-o.
Повний текст джерелаKobayashi, Yuichi, Yuji Nakayama, and Shinya Yoshida. "Determination of the stereoisomer of korormicin from eight possible stereoisomers by total synthesis." Tetrahedron Letters 41, no. 9 (February 2000): 1465–68. http://dx.doi.org/10.1016/s0040-4039(99)02319-9.
Повний текст джерелаTimperley, Christopher M., Jonathan E. Forman, Mohammad Abdollahi, Abdullah Saeed Al-Amri, Isel Pascual Alonso, Augustin Baulig, Veronica Borrett, et al. "Advice from the Scientific Advisory Board of the Organisation for the Prohibition of Chemical Weapons on isotopically labelled chemicals and stereoisomers in relation to the Chemical Weapons Convention." Pure and Applied Chemistry 90, no. 10 (October 25, 2018): 1647–70. http://dx.doi.org/10.1515/pac-2018-0803.
Повний текст джерелаYakovleva, M. P., V. A. Vydrina, N. M. Ishmuratova, and G. Yu Ishmuratov. "CONTRIBUTION OF UFA SCIENTISTS TO THE CHEMISTRY OF OPTICALLY ACTIVE SEX PHEROMONE OF PINE SAWFLIES." ÈKOBIOTEH 3, no. 4 (2020): 634–42. http://dx.doi.org/10.31163/2618-964x-2020-3-4-634-642.
Повний текст джерелаZaikin, Vladimir G., and Roman S. Borisov. "Stereospecific Ion—molecule Reactions in the Trans-Decahydro-4-Hydroxyquinoline Series upon Chemical Ionization." European Journal of Mass Spectrometry 8, no. 2 (April 2002): 139–45. http://dx.doi.org/10.1255/ejms.482.
Повний текст джерелаMorikawa, Atsushi, Masa-Aki Kakimoto, and Yoshio Imai. "Preparation of aromatic polyamides from newly separated optically pure phenylindanedicarboxylic acid and their application to enantioseparation." High Performance Polymers 6, no. 4 (August 1994): 415–21. http://dx.doi.org/10.1088/0954-0083/6/4/009.
Повний текст джерелаBrem, Jürgen, Sander S. van Berkel, David Zollman, Sook Y. Lee, Opher Gileadi, Peter J. McHugh, Timothy R. Walsh, Michael A. McDonough та Christopher J. Schofield. "Structural Basis of Metallo-β-Lactamase Inhibition by Captopril Stereoisomers". Antimicrobial Agents and Chemotherapy 60, № 1 (19 жовтня 2015): 142–50. http://dx.doi.org/10.1128/aac.01335-15.
Повний текст джерелаMeglia, Guillermo E., Søren K. Jensen, Charlotte Lauridsen та Karin Persson Waller. "α-Tocopherol concentration and stereoisomer composition in plasma and milk from dairy cows fed natural or synthetic vitamin E around calving". Journal of Dairy Research 73, № 2 (30 березня 2006): 227–34. http://dx.doi.org/10.1017/s0022029906001701.
Повний текст джерелаLuong, Thanh-Truc, Guylain Boulay, and Gaétan Guillemette. "Study on the stereoselectivity of Inositol 1,4,5-trisphosphate recognition sites of bovine adrenal cortex." Canadian Journal of Physiology and Pharmacology 70, no. 4 (April 1, 1992): 434–41. http://dx.doi.org/10.1139/y92-055.
Повний текст джерелаMosandl, Armin, Uwe Hener, and Heinz-Dieter Fenske. "Stereoisomere Aromastoffe, XXXI Tetrahydro-2-methylthiophen-3-ol - Struktur und Eigenschaften der Stereoisomeren." Liebigs Annalen der Chemie 1989, no. 9 (September 13, 1989): 859–62. http://dx.doi.org/10.1002/jlac.198919890237.
Повний текст джерелаDiukendjieva, Antonia, Merilin Al Sharif, Petko Alov, Tania Pencheva, Ivanka Tsakovska, and Ilza Pajeva. "ADME/Tox Properties and Biochemical Interactions of Silybin Congeners: In silico Study." Natural Product Communications 12, no. 2 (February 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200208.
Повний текст джерелаJaneba, Zlatko, Antonín Holý, Hana Votavová, and Milena Masojídková. "Intramolecular Cyclization of Some Acyclic Nucleoside Analogs." Collection of Czechoslovak Chemical Communications 61, no. 3 (1996): 442–57. http://dx.doi.org/10.1135/cccc19960442.
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