Статті в журналах з теми "13C NMR identification"
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S. Clendinen, Chaevien, Gregory S. Stupp, Bing Wang, Timothy J. Garrett, and Arthur S. Edison. "13C Metabolomics: NMR and IROA for Unknown Identification." Current Metabolomics 4, no. 2 (June 30, 2016): 116–20. http://dx.doi.org/10.2174/2213235x04666160407212156.
Повний текст джерелаChamberlain, Paul H. "Identification of an Alcohol with 13C NMR Spectroscopy." Journal of Chemical Education 90, no. 10 (September 20, 2013): 1365–67. http://dx.doi.org/10.1021/ed300833s.
Повний текст джерелаBuděšínský, Miloš, and David Šaman. "Identification of acyl groups occurring in sesquiterpene lactones: Proton and carbon-13 NMR study." Collection of Czechoslovak Chemical Communications 52, no. 2 (1987): 453–75. http://dx.doi.org/10.1135/cccc19870453.
Повний текст джерелаStřešinková, Dagmar, František Halmo, and Tibor Liptaj. "Computer Assisted 13C NMR Identification of Components of Complex Organic Mixtures: Byproducts in the Manufacture of Cyclohexanone." Collection of Czechoslovak Chemical Communications 57, no. 10 (1992): 2095–99. http://dx.doi.org/10.1135/cccc19922095.
Повний текст джерелаFerrante, Laura, Kashif Rajpoot, Mark Jeeves, and Christian Ludwig. "Automated analysis for multiplet identification from ultra-high resolution 2D-1H,13C-HSQC NMR spectra." Wellcome Open Research 7 (October 14, 2022): 262. http://dx.doi.org/10.12688/wellcomeopenres.18248.1.
Повний текст джерелаKartashov, V. S. "13C NMR identification of drugs based on pyridine derivatives." Pharmaceutical Chemistry Journal 33, no. 2 (February 1999): 113. http://dx.doi.org/10.1007/bf02508121.
Повний текст джерелаLizotte, Pauline A., and Jonathan E. Poulton. "Identification of (R)-Vicianin in Davallia trichomanoides Blume." Zeitschrift für Naturforschung C 41, no. 1-2 (February 1, 1986): 5–8. http://dx.doi.org/10.1515/znc-1986-1-202.
Повний текст джерелаMeese, Claus O., та Peter Fischer. "Tracing the Human Metabolism of Stable Isotope-Labelled Drugs by ex vivo NM R Spectroscopy A Revision of S-Carboxymethyl-ʟ-cysteine Biotransformation". Zeitschrift für Naturforschung C 45, № 11-12 (1 грудня 1990): 1171–75. http://dx.doi.org/10.1515/znc-1990-11-1215.
Повний текст джерелаEshimbetov, Alisher, Shahobiddin Adizov, Inderpreet Kaur, and Akhmed Reymov. "Is it possible to differentiate between 2-phenylaminodihydro-1,3-thiazine from 2-phenyliminotetrahydro-1,3-thiazine by spectral methods? New glance to the old problem." European Journal of Chemistry 12, no. 1 (March 31, 2021): 77–80. http://dx.doi.org/10.5155/eurjchem.12.1.77-80.2068.
Повний текст джерелаMoiseev, S. V., N. E. Kuz’mina, and A. I. Luttseva. "Development of Identification Test Methods for Triptorelin Acetate and Goserelin Acetate Substances using NMR spectroscopy." Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products 9, no. 1 (March 25, 2019): 54–63. http://dx.doi.org/10.30895/1991-2919-2019-9-1-54-63.
Повний текст джерелаCanton, Marine, Jane Hubert, Stéphane Poigny, Richard Roe, Yves Brunel, Jean-Marc Nuzillard, and Jean-Hugues Renault. "Dereplication of Natural Extracts Diluted in Glycerin: Physical Suppression of Glycerin by Centrifugal Partition Chromatography Combined with Presaturation of Solvent Signals in 13C-Nuclear Magnetic Resonance Spectroscopy." Molecules 25, no. 21 (October 31, 2020): 5061. http://dx.doi.org/10.3390/molecules25215061.
Повний текст джерелаKuz’mina, Natalia E., Sergey V. Moiseev, Elena Y. Severinova, Evgenii A. Stepanov, and Natalia D. Bunyatyan. "Identification and Quantification by NMR Spectroscopy of the 22R and 22S Epimers in Budesonide Pharmaceutical Forms." Molecules 27, no. 7 (March 31, 2022): 2262. http://dx.doi.org/10.3390/molecules27072262.
Повний текст джерелаGarcia, Gabriel, Delphin Rabehaja, Julie-Marie Charmillon, Panja Ramanoelina, Joseph Casanova, and Félix Tomi. "Integrated Analysis of the Bark Oil from Cinnamosma madagascariensis by GC(RI), GC-MS and NMR. 13C NMR data of Cyclocopacamphene and Cyclosativene." Natural Product Communications 12, no. 2 (February 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200235.
Повний текст джерелаVijay, Dhanya, Nassra S. Alshamsi, Ziad Moussa, and M. Kalim Akhtar. "Extraction of the Anticancer and Antimicrobial Agent, Prodigiosin, from Vibrio gazogenes PB1 and Its Identification by 1D and 2D NMR." Molecules 27, no. 18 (September 16, 2022): 6030. http://dx.doi.org/10.3390/molecules27186030.
Повний текст джерелаKINOSHITA, Haruki, Yasuo TOHIRA, Hiroshi SUGIYAMA, and Mikio SAWADA. "Use of 13C-NMR Spectroscopy for Detection and Identification of Labile Metabolites of 13C-labeled Inabenfide." Journal of Pesticide Science 12, no. 2 (1987): 261–63. http://dx.doi.org/10.1584/jpestics.12.261.
Повний текст джерелаIrmawan, Muhammad, Frederyk Mandey, and Seniwati Dali. "Isolation, Identification, Characteriterization, And Toxicity Essay Of Non-polar Secondary Metabolite Fraction From Ageratum conyzoides L." Indo. J. Chem. Res. 6, no. 1 (July 31, 2018): 513–17. http://dx.doi.org/10.30598//ijcr.2018.6.1.
Повний текст джерелаIrmawan, Muhammad, Frederyk Mandey, and Seniwati Dali. "Isolation, Identification, Characteriterization, And Toxicity Essay Of Non-polar Secondary Metabolite Fraction From Ageratum conyzoides L." Indo. J. Chem. Res. 6, no. 1 (July 31, 2018): 513–17. http://dx.doi.org/10.30598/v12.
Повний текст джерелаHung, Nguyen Huy. "CHEMICAL CONSTITUENTS FROM THE SEEDS OF ANNONA RETICULATA L. IN VIETNAM." Vietnam Journal of Science and Technology 54, no. 4A (March 21, 2018): 221. http://dx.doi.org/10.15625/2525-2518/54/4a/11997.
Повний текст джерелаKanzari-Mnallah, Dorra, Med L. Efrit, Jiří Pavlíček, Frédéric Vellieux, Habib Boughzala, and Azaiez B. Akacha. "Synthesis, Conformational Analysis and Crystal Structure of New Thioxo, Oxo, Seleno Diastereomeric Cyclophosphamides Containing 1,3,2-dioxaphosphorinane." Current Organic Chemistry 23, no. 2 (April 23, 2019): 205–13. http://dx.doi.org/10.2174/1385272823666190213142748.
Повний текст джерелаBakibaev, A. A., М. Zh Sadvakassova, R. Sh Еrkasov, and А. Е. Аtagulova. "Identification and analysis of N-alkyl-N’-arylalkylureas by nuclear magnetic resonance." BULLETIN of the L.N. Gumilyov Eurasian National University. Chemistry. Geography. Ecology Series 130, no. 1 (2020): 18–22. http://dx.doi.org/10.32523/2616-6771-2020-130-1-18-22.
Повний текст джерелаZabala, Myrnille Joy B., Lolita G. Lagurin, and Fabian M. Dayrit. "13C Nuclear Magnetic Resonance Phytochemical Profiling of the In Vitro Antidiabetic Potential of Vitex negundo L." Abstract Proceedings International Scholars Conference 4, no. 1 (August 16, 2019): 181. http://dx.doi.org/10.35974/isc.v4i1.1652.
Повний текст джерелаMesilaakso, Markku, Eeva-Liisa Tolppa, and Paula Nousiainen. "Analysis of 1H and 13C{1H} NMR Spectral Parameters of Diphenylchloroarsine, Diphenylcyanoarsine, and 10-Chloro- 5,10-Dihydrophenarsazine: Identification of the Compounds through Reference to Simulated Spectra." Applied Spectroscopy 51, no. 5 (May 1997): 733–37. http://dx.doi.org/10.1366/0003702971940891.
Повний текст джерелаKeller, Julia, Luisa Hantschke, Hajo Haase, and Matthias Koch. "Synthesis and Structural Identification of a Biaryl Ether-Linked Zearalenone Dimer." Molecules 23, no. 10 (October 12, 2018): 2624. http://dx.doi.org/10.3390/molecules23102624.
Повний текст джерелаNyigo, Vitus A., Hamisi M. Malebo, Faith Mabiki, and Robinson Mdegela. "Isolation and identification of long -chain aliphatic compounds from Synadenium glaucescens." Journal of Phytopharmacology 11, no. 3 (June 25, 2022): 151–54. http://dx.doi.org/10.31254/phyto.2022.11303.
Повний текст джерелаOuattara, Zana A., Jean Brice Boti, Coffy Antoine Ahibo, Félix Tomi, Joseph Casanova, and Ange Bighelli. "Combined Analysis of the Root Bark Oil of Cleistopholis glauca by Chromatographic and Spectroscopic Techniques." Natural Product Communications 8, no. 12 (December 2013): 1934578X1300801. http://dx.doi.org/10.1177/1934578x1300801231.
Повний текст джерелаBecette, Owen B., Guanghui Zong, Bin Chen, Kehinde M. Taiwo, David A. Case, and T. Kwaku Dayie. "Solution NMR readily reveals distinct structural folds and interactions in doubly 13C- and 19F-labeled RNAs." Science Advances 6, no. 41 (October 2020): eabc6572. http://dx.doi.org/10.1126/sciadv.abc6572.
Повний текст джерелаKAWAI, Shigeru, Kanzo SAKATA, Akihito YAGI, and Kazuo INA. "Identification of New Constituents of Cider Vineger by 13C-NMR Spectroscopic Study." Agricultural and Biological Chemistry 55, no. 10 (1991): 2633–35. http://dx.doi.org/10.1271/bbb1961.55.2633.
Повний текст джерелаChalmers, A. A., and P. Perlstein. "Identification of hardeners in solid epoxy resins by high-resolution 13C-NMR." European Polymer Journal 23, no. 11 (January 1987): 887–90. http://dx.doi.org/10.1016/0014-3057(87)90063-2.
Повний текст джерелаdo Nascimento Marinho, Rosiane Ferreira, Bianca Roberta Peres Angrisani, Arthur Ladeira Macedo, Davyson de Lima Moreira, Carlos Magno Rocha Ribeiro, Thatyana Rocha Alves Vasconcelos, and Alessandra Leda Valverde. "1H and 13C NMR Spectral Data of Neolignans Isolated from Piper Species." Current Organic Chemistry 24, no. 14 (October 13, 2020): 1527–54. http://dx.doi.org/10.2174/1385272824999200608133542.
Повний текст джерелаSauter, F., E. W. H. Hayek, W. Moche, and U. Jordis. "Betulin aus archäologischem Schwelteer / Identification of Betulin in Archaeological Tar." Zeitschrift für Naturforschung C 42, no. 11-12 (December 1, 1987): 1151–52. http://dx.doi.org/10.1515/znc-1987-11-1202.
Повний текст джерелаNyigo, Vitus A., Xolani Peter, Faith Mabiki, Hamisi M. Malebo, Robinson H. Mdegela та Gerda Fouche. "Isolation and identification of euphol and β-sitosterol from the dichloromethane extracts of Synadenium glaucescens". Journal of Phytopharmacology 5, № 3 (3 серпня 2016): 100–104. http://dx.doi.org/10.31254/phyto.2016.5302.
Повний текст джерелаDjié Bi, Tra Marc Gabin, Acafou Thierry Yapi, Zana Adama Ouattara, Janat Akhanovna Mamyrbekova-Békro, Mathieu Paoli, Félix Tomi, Vincent Castola, and Ange Bighelli. "Composition and Variability of Leaf Oil from Monodora Crispata -13C NMR Identification of Heat-sensitive Compounds." Natural Product Communications 12, no. 3 (March 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200332.
Повний текст джерелаMarliyana, Soerya Dewi, Muhamad Widyo Wartono, Fajar Rakhman Wibowo, and Gesti Munasah. "Isolasi dan Identifikasi Senyawa Seskuiterpen dari Curcuma soloensis Val. (Temu Glenyeh)." Jurnal Kimia VALENSI 4, no. 2 (November 30, 2018): 137–42. http://dx.doi.org/10.15408/jkv.v4i2.7443.
Повний текст джерелаSaidi, Nurdin, A. Hamid A. Hadi, Khalijah Awang, and Mat Ropi Mukhtar. "APHORPINE ALKALOIDS FROM BARK OF Cryptocarya ferrea." Indonesian Journal of Chemistry 9, no. 3 (June 24, 2010): 461–65. http://dx.doi.org/10.22146/ijc.21516.
Повний текст джерелаJankowski, C. K., M. R. Van Calsteren, N. Aychet, J. F. Dozol, C. Moulin, and C. Lamouroux. "Study of the nitration of di-n-octylcrown-6 calix[4]arene using LCMS, NMR, and molecular modelling." Canadian Journal of Chemistry 83, no. 8 (August 1, 2005): 1098–113. http://dx.doi.org/10.1139/v05-126.
Повний текст джерелаRibeiro, Carlos Magno Rocha, Thiago Silva Galvão de Souza, Karinne Canevalli de Almeida, Karen Danielle Borba Dutra, and Alessandra Leda Valverde. "Heliannuol: Distribution, Biological Activities, 1H and 13C-NMR Spectral Data." Mini-Reviews in Organic Chemistry 17, no. 3 (April 28, 2020): 309–22. http://dx.doi.org/10.2174/1570193x16666190405102658.
Повний текст джерелаRumampuk, Rymond J. "IDENTIFICATION AND SEQUENCING BY NMR SPECTROSCOPY OF THE CARBOHYDRATE MOIETY IN A SAPONIN FROM Barringtonia asiatica." Indonesian Journal of Chemistry 1, no. 3 (June 5, 2010): 120–24. http://dx.doi.org/10.22146/ijc.21936.
Повний текст джерелаPalu, Doreen, Ange Bighelli, Joseph Casanova, and Mathieu Paoli. "Identification and Quantitation of Ursolic and Oleanolic Acids in Ilex aquifolium L. Leaf Extracts Using 13C and 1H-NMR Spectroscopy." Molecules 24, no. 23 (December 3, 2019): 4413. http://dx.doi.org/10.3390/molecules24234413.
Повний текст джерелаPoulhazan, Alexandre, Alexandre Arnold, Dror Warschawski, and Isabelle Marcotte. "Unambiguous Ex Situ and in Cell 2D 13C Solid-State NMR Characterization of Starch and Its Constituents." International Journal of Molecular Sciences 19, no. 12 (November 30, 2018): 3817. http://dx.doi.org/10.3390/ijms19123817.
Повний текст джерелаShahriar, Mohammad Shahriar, Mohiuddin Ahmed Bhuiyan, and Md Sohel Rana. "Isolation and identification of different compounds from Citrus assamensis leaf." Journal of Bangladesh Academy of Sciences 44, no. 2 (January 19, 2021): 85–93. http://dx.doi.org/10.3329/jbas.v44i2.51453.
Повний текст джерелаAtun, Sri, Nurfina Aznama, Retno Arianingrum, and Masatake Niwab. "STRUCTURE IDENTIFICATION OF A TRIMER STILBENOID COMPOUND FROM STEM BARK Hopea nigra (DIPTEROCARPACEAE)." Indonesian Journal of Chemistry 5, no. 3 (June 15, 2010): 211–14. http://dx.doi.org/10.22146/ijc.21791.
Повний текст джерелаSiivari, Jari, Arto Maaninen, Esa Haapaniemi, Risto S. Laitinen, and Tristram Chivers. "Formation and Identification of Bis[bis(trimethylsilyl)amino]triand tetrachalcogenides." Zeitschrift für Naturforschung B 50, no. 11 (November 1, 1995): 1575–82. http://dx.doi.org/10.1515/znb-1995-1101.
Повний текст джерелаDi Pietro, Maria Enrica, Alberto Mannu, and Andrea Mele. "NMR Determination of Free Fatty Acids in Vegetable Oils." Processes 8, no. 4 (March 31, 2020): 410. http://dx.doi.org/10.3390/pr8040410.
Повний текст джерелаBakibaev, А. А., М. Zh Sadvakassova, V. S. Malkov, R. Sh Еrkasov, A. A. Sorvanov, and O. A. Kotelnikov. "Study of the biologically active acyclic ureas by nuclear magnetic resonance." Bulletin of the Karaganda University. "Chemistry" series 100, no. 4 (December 30, 2020): 60–74. http://dx.doi.org/10.31489/2020ch4/60-74.
Повний текст джерелаFerreira, Marcelo J. P., Francimeiry C. Oliveira, Sandra A. V. Alvarenga, Patrı́cia A. T. Macari, Gilberto V. Rodrigues, and Vicente P. Emerenciano. "Automatic identification by 13C NMR of substituent groups bonded in natural product skeletons." Computers & Chemistry 26, no. 6 (November 2002): 601–32. http://dx.doi.org/10.1016/s0097-8485(02)00029-3.
Повний текст джерелаMoore, Jeremy K., J. Andrew Surface, Allison Brenner, Philip Skemer, Mark S. Conradi, and Sophia E. Hayes. "Quantitative Identification of Metastable Magnesium Carbonate Minerals by Solid-State 13C NMR Spectroscopy." Environmental Science & Technology 49, no. 1 (December 17, 2014): 657–64. http://dx.doi.org/10.1021/es503390d.
Повний текст джерелаNam, Anne-Marie, Mathieu Paoli, Vincent Castola, Joseph Casanova, and Ange Bighelli. "Identification and Quantitative Determination of Lignans in Cedrus atlantica Resins using 13C NMR Spectroscopy." Natural Product Communications 6, no. 3 (March 2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600316.
Повний текст джерелаKazalaki, Aristea, Maria Misiak, Apostolos Spyros, and Photis Dais. "Identification and quantitative determination of carbohydrate molecules in Greek honey by employing 13C NMR spectroscopy." Analytical Methods 7, no. 14 (2015): 5962–72. http://dx.doi.org/10.1039/c5ay01243k.
Повний текст джерелаIrmawan, Muhammad, Frederyk Mandey, and Seniwati Dali. "Isolasi, Identifikasi, Karakterisasi Dan Uji Toksisitas Senyawa Metabolit Sekunder Fraksi Nonpolar Akar Babandotan (Ageratum conyzoides L)." Indo. J. Chem. Res. 6, no. 1 (July 31, 2018): 1–5. http://dx.doi.org/10.30598//ijcr.2018.6-muh.
Повний текст джерелаBISHOP, G. Reid, Zhenyu ZHU, L. Tracy WHITEHEAD, P. Rickey HICKS, and L. Victor DAVIDSON. "Identification of reaction products and intermediates of aromatic-amine dehydrogenase by 15N and 13C NMR." Biochemical Journal 330, no. 3 (March 15, 1998): 1159–63. http://dx.doi.org/10.1042/bj3301159.
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