Artículos de revistas sobre el tema "Stereoisomeri"
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Costa, Maria L. M., Miguel Borges, Evaldo F. Vilela, Paulo de Marco Jr y 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, n.º 3 (septiembre de 2000): 413–22. http://dx.doi.org/10.1590/s0301-80592000000300004.
Texto completoLapčík, Oldřich, Richard Hampl, Martin Hill, Luboslav Stárka, Alexander Kasal, Vladimír Pouzar y Zdeněk Putz. "Radioimmunological and Chromatographic Properties of Tyrosine Methyl Ester Conjugates with Stereoisomeric Steroid Carboxy Derivatives". Collection of Czechoslovak Chemical Communications 61, n.º 5 (1996): 799–807. http://dx.doi.org/10.1135/cccc19960799.
Texto completoKuchan, Matthew J., Søren K. Jensen, Elizabeth J. Johnson y 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, n.º 1 (16 de mayo de 2016): 126–31. http://dx.doi.org/10.1017/s0007114516001719.
Texto completoSheikh, Ishfaq Ahmad y Mohd Amin Beg. "Structural Aspects of Potential Endocrine-Disrupting Activity of Stereoisomers for a Common Pesticide Permethrin against Androgen Receptor". Biology 10, n.º 2 (11 de febrero de 2021): 143. http://dx.doi.org/10.3390/biology10020143.
Texto completoDIEUAIDE-NOUBHANI, Martine, Stanny ASSELBERGHS, Guy P. MANNAERTS y 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, n.º 2 (15 de julio de 1997): 367–73. http://dx.doi.org/10.1042/bj3250367.
Texto completoDersjant-Li, Jensen, Bos y 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, n.º 4 (1 de julio de 2009): 199–211. http://dx.doi.org/10.1024/0300-9831.79.4.199.
Texto completoTirri, 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, n.º 16 (16 de agosto de 2021): 8771. http://dx.doi.org/10.3390/ijms22168771.
Texto completoCortinas, Lucia, Ana Barroeta, Jaume Galobart y Søren K. Jensen. "Distribution of α-tocopherol stereoisomers in liver and thigh of chickens". British Journal of Nutrition 92, n.º 2 (agosto de 2004): 295–301. http://dx.doi.org/10.1079/bjn20041188.
Texto completoHymøller, Lone, Saman Lashkari, Tove N. Clausen y 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, n.º 12 (17 de octubre de 2018): 1332–37. http://dx.doi.org/10.1017/s0007114518002878.
Texto completoBrice-Tutt, Ariana C., Sanjeewa N. Senadheera, Michelle L. Ganno, Shainnel O. Eans, Tanvir Khaliq, Thomas F. Murray, Jay P. McLaughlin y Jane V. Aldrich. "Phenylalanine Stereoisomers of CJ-15,208 and [d-Trp]CJ-15,208 Exhibit Distinctly Different Opioid Activity Profiles". Molecules 25, n.º 17 (2 de septiembre de 2020): 3999. http://dx.doi.org/10.3390/molecules25173999.
Texto completoLicea Perez, Hermes y Clara Andonian. "Chemical derivatization in combination with supercritical fluid chromatography to improve resolution of stereoisomers". Bioanalysis 13, n.º 12 (junio de 2021): 985–99. http://dx.doi.org/10.4155/bio-2021-0053.
Texto completoPerlikowska, Wiesława, Remigiusz Żurawiński y Marian Mikołajczyk. "A new and expeditious synthesis of all enantiomerically pure stereoisomers of rosaprostol, an antiulcer drug". Beilstein Journal of Organic Chemistry 12 (21 de octubre de 2016): 2234–39. http://dx.doi.org/10.3762/bjoc.12.215.
Texto completoPresini, Francesco, Graziano Di Carmine, Pier Paolo Giovannini, Virginia Cristofori, Lindomar Alberto Lerin, Olga Bortolini, Claudio Trapella y Anna Fantinati. "Chemoenzymatic Stereodivergent Synthesis of All the Possible Stereoisomers of the 2,3-Dimethylglyceric Acid Ethyl Ester". Catalysts 11, n.º 12 (26 de noviembre de 2021): 1440. http://dx.doi.org/10.3390/catal11121440.
Texto completoJia, Qi, Nana Xu, Pengqian Mu, Bo Wang, Shuming Yang y 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.
Texto completoMcIntosh, John M. y Ivy E. E. Hayes. "Stereochemistry of 3-carboxylated 2,5-dihydrothiophene formation". Canadian Journal of Chemistry 65, n.º 1 (1 de enero de 1987): 110–13. http://dx.doi.org/10.1139/v87-018.
Texto completoDuong-Thi, Minh-Dao, Maria Bergström, Tomas Fex, Susanne Svensson, Sten Ohlson y Roland Isaksson. "Weak Affinity Chromatography for Evaluation of Stereoisomers in Early Drug Discovery". Journal of Biomolecular Screening 18, n.º 6 (11 de marzo de 2013): 748–55. http://dx.doi.org/10.1177/1087057113480391.
Texto completoPham, Hoai, Madelyn Hunsley, Chou-Hsun Yang, Haobin Wang y Scott M. Reed. "Demonstration of a Stereospecific Photochemical Meta Effect". Photochem 2, n.º 1 (12 de enero de 2022): 69–76. http://dx.doi.org/10.3390/photochem2010006.
Texto completoCastillo-Aguirre, Alver A., Zuly Jenny Rivera Monroy y 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 (16 de abril de 2019): 1–6. http://dx.doi.org/10.1155/2019/2051282.
Texto completoLandge, Shashikant B., Sanjay A. Jadhav, Sunil B. Dahale, Navanath C. Niphade, Ch Lakshmi Narayana, Vishwas B. Gaikwad y 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 (21 de octubre de 2011): 1–7. http://dx.doi.org/10.4061/2011/243491.
Texto completoTonoi, 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, n.º 19 (22 de septiembre de 2019): 3437. http://dx.doi.org/10.3390/molecules24193437.
Texto completoRousselin, Yoann, Hugo Laureano y Alexandre Clavel. "Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman". Acta Crystallographica Section E Crystallographic Communications 71, n.º 8 (8 de julio de 2015): o552—o553. http://dx.doi.org/10.1107/s205698901501261x.
Texto completoKuchan, Matthew J., Katherine M. Ranard, Priyankar Dey, Sookyoung Jeon, Geoff Y. Sasaki, Karen J. Schimpf, Richard S. Bruno, Martha Neuringer y 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, n.º 9 (2 de julio de 2020): 2305–13. http://dx.doi.org/10.1093/jn/nxaa174.
Texto completoFUJITA, Shinsaku. "RS-Stereoisomeric Groups and Enumeration of Quadruplets of RS-Stereoisomers". Journal of Computer Chemistry, Japan 13, n.º 3 (2014): 155–56. http://dx.doi.org/10.2477/jccj.2014-0014.
Texto completoIl`in, E. G., A. S. Parshakov, V. G. Yarzhemsky, E. A. Ugolkova, L. V. Goyeva y V. I. Privalov. "Physical chemistry CeF4 complexes in organic solvents". Доклады Академии наук 488, n.º 1 (24 de septiembre de 2019): 47–51. http://dx.doi.org/10.31857/s0869-5652488147-51.
Texto completoBencke, Carlos, Mário Marangoni, Adriano Camargo, Cassio Fantinel, Helio Bonacorso, Marcos Martins y Nilo Zanatta. "Synthesis of Penta-2,4-dienenitriles by the Horner–Wadsworth–Emmons Olefination of Enones". Synthesis 49, n.º 23 (24 de agosto de 2017): 5131–42. http://dx.doi.org/10.1055/s-0036-1590871.
Texto completoKIDANE, A., I. L. NESHEIM, H. J. S. LARSEN, E. THUEN, S. K. JENSEN y 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, n.º 5 (18 de marzo de 2015): 929–42. http://dx.doi.org/10.1017/s0021859615000052.
Texto completoAnderbrant, Olle, D. Barry Lyons, Joakim Bång, Erik Hedenström y 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, n.º 10 (29 de septiembre de 2021): 886. http://dx.doi.org/10.3390/insects12100886.
Texto completoFujita, 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, n.º 2 (2022): 239–318. http://dx.doi.org/10.46793/match.88-2.239f.
Texto completoXu, Yangrong, Hangjun Tang, Yijie Xu, Jialin Guo, Xu Zhao, Qingguo Meng y 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, n.º 10 (22 de mayo de 2022): 3335. http://dx.doi.org/10.3390/molecules27103335.
Texto completoLeitgeb, Balázs. "Spatial relationships between the pharmacophores of endomorphin-2: a comparative study of stereoisomers". Open Chemistry 10, n.º 6 (1 de diciembre de 2012): 1791–98. http://dx.doi.org/10.2478/s11532-012-0105-3.
Texto completoBernát, Juraj, Ladislav Kniežo, Gabriela Birošová, Miloš Buděšínský, Jaroslav Podlaha, Jana Podlahová y 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, n.º 6 (1992): 1299–313. http://dx.doi.org/10.1135/cccc19921299.
Texto completoBrine, G. A., F. I. Carroll, T. M. Richardson-Leibert, H. Xu y R. B. Rothman. "Ohmefentanyl and Its Stereoisomers: Chemistry and Pharmacology". Current Medicinal Chemistry 4, n.º 4 (agosto de 1997): 247–70. http://dx.doi.org/10.2174/0929867304666220313115017.
Texto completoOzenil, Marius, Jonas Aronow, Daniela Piljak, Chrysoula Vraka, Wolfgang Holzer, Helmut Spreitzer, Wolfgang Wadsak, Marcus Hacker y Verena Pichler. "Synthesis, Biological, and Computational Evaluation of Antagonistic, Chiral Hydrobenzoin Esters of Arecaidine Targeting mAChR M1". Pharmaceuticals 13, n.º 12 (30 de noviembre de 2020): 437. http://dx.doi.org/10.3390/ph13120437.
Texto completoJežek, Rudolf, Miroslava Žertová, Jiřina Slaninová, Pavel Majer y Zdenko Procházka. "Antagonistic Analogs of Oxytocin with Substituted Phenylalanine or Tyrosine in Position 2". Collection of Czechoslovak Chemical Communications 59, n.º 6 (1994): 1430–38. http://dx.doi.org/10.1135/cccc19941430.
Texto completoPolívka, Zdeněk, Jiří Holubek, Emil Svátek, Jan Metyš y 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, n.º 5 (1985): 1078–88. http://dx.doi.org/10.1135/cccc19851078.
Texto completoGill, Brendon D., Jackie E. Wood y Harvey E. Indyk. "Analysis of α-Tocopherol Stereoisomers in Fortified Infant Formula by Chiral Chromatography". Journal of AOAC INTERNATIONAL 104, n.º 3 (23 de enero de 2021): 725–31. http://dx.doi.org/10.1093/jaoacint/qsab012.
Texto completoHenthorn, Thomas K., Tom C. Krejcie, Claus U. Niemann, Cheri Enders-Klein, Colin A. Shanks y Michael J. Avram. "Ketamine Distribution Described by a Recirculatory Pharmacokinetic Model Is Not Stereoselective". Anesthesiology 91, n.º 6 (1 de diciembre de 1999): 1733. http://dx.doi.org/10.1097/00000542-199912000-00027.
Texto completoReichert, Sylvia, Matthias Wüst, Thomas Beck y Armin Mosandl. "Stereoisomeric Flavor Compounds LXXXI: Dill Ether and Itscis-Stereoisomers: Synthesis and Enantioselective Analysis". Journal of High Resolution Chromatography 21, n.º 3 (1 de marzo de 1998): 185–88. http://dx.doi.org/10.1002/(sici)1521-4168(19980301)21:3<185::aid-jhrc185>3.0.co;2-j.
Texto completoReichert, Sylvia y Armin Mosandl. "Stereoisomeric Flavor Compounds LXXXII Dill Ether and Its Stereoisomers: Synthesis and Enantioselective Analysis". Journal of High Resolution Chromatography 22, n.º 11 (1 de noviembre de 1999): 631–34. http://dx.doi.org/10.1002/(sici)1521-4168(19991101)22:11<631::aid-jhrc631>3.0.co;2-o.
Texto completoKobayashi, Yuichi, Yuji Nakayama y Shinya Yoshida. "Determination of the stereoisomer of korormicin from eight possible stereoisomers by total synthesis". Tetrahedron Letters 41, n.º 9 (febrero de 2000): 1465–68. http://dx.doi.org/10.1016/s0040-4039(99)02319-9.
Texto completoTimperley, 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, n.º 10 (25 de octubre de 2018): 1647–70. http://dx.doi.org/10.1515/pac-2018-0803.
Texto completoYakovleva, M. P., V. A. Vydrina, N. M. Ishmuratova y G. Yu Ishmuratov. "CONTRIBUTION OF UFA SCIENTISTS TO THE CHEMISTRY OF OPTICALLY ACTIVE SEX PHEROMONE OF PINE SAWFLIES". ÈKOBIOTEH 3, n.º 4 (2020): 634–42. http://dx.doi.org/10.31163/2618-964x-2020-3-4-634-642.
Texto completoZaikin, Vladimir G. y Roman S. Borisov. "Stereospecific Ion—molecule Reactions in the Trans-Decahydro-4-Hydroxyquinoline Series upon Chemical Ionization". European Journal of Mass Spectrometry 8, n.º 2 (abril de 2002): 139–45. http://dx.doi.org/10.1255/ejms.482.
Texto completoMorikawa, Atsushi, Masa-Aki Kakimoto y Yoshio Imai. "Preparation of aromatic polyamides from newly separated optically pure phenylindanedicarboxylic acid and their application to enantioseparation". High Performance Polymers 6, n.º 4 (agosto de 1994): 415–21. http://dx.doi.org/10.1088/0954-0083/6/4/009.
Texto completoBrem, Jürgen, Sander S. van Berkel, David Zollman, Sook Y. Lee, Opher Gileadi, Peter J. McHugh, Timothy R. Walsh, Michael A. McDonough y Christopher J. Schofield. "Structural Basis of Metallo-β-Lactamase Inhibition by Captopril Stereoisomers". Antimicrobial Agents and Chemotherapy 60, n.º 1 (19 de octubre de 2015): 142–50. http://dx.doi.org/10.1128/aac.01335-15.
Texto completoMeglia, Guillermo E., Søren K. Jensen, Charlotte Lauridsen y 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, n.º 2 (30 de marzo de 2006): 227–34. http://dx.doi.org/10.1017/s0022029906001701.
Texto completoLuong, Thanh-Truc, Guylain Boulay y 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, n.º 4 (1 de abril de 1992): 434–41. http://dx.doi.org/10.1139/y92-055.
Texto completoMosandl, Armin, Uwe Hener y Heinz-Dieter Fenske. "Stereoisomere Aromastoffe, XXXI Tetrahydro-2-methylthiophen-3-ol - Struktur und Eigenschaften der Stereoisomeren". Liebigs Annalen der Chemie 1989, n.º 9 (13 de septiembre de 1989): 859–62. http://dx.doi.org/10.1002/jlac.198919890237.
Texto completoDiukendjieva, Antonia, Merilin Al Sharif, Petko Alov, Tania Pencheva, Ivanka Tsakovska y Ilza Pajeva. "ADME/Tox Properties and Biochemical Interactions of Silybin Congeners: In silico Study". Natural Product Communications 12, n.º 2 (febrero de 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200208.
Texto completoJaneba, Zlatko, Antonín Holý, Hana Votavová y Milena Masojídková. "Intramolecular Cyclization of Some Acyclic Nucleoside Analogs". Collection of Czechoslovak Chemical Communications 61, n.º 3 (1996): 442–57. http://dx.doi.org/10.1135/cccc19960442.
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