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Shyshkanov, Sergey A., Orlov, Nikolai V. (2016) Design of Selenium-Based Chiral Chemical Probes for Simultaneous Enantio- and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy. Chemistry - A European Journal, 22 (43). 15458-15467 doi:10.1002/chem.201602884

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Reference TypeJournal (article/letter/editorial)
TitleDesign of Selenium-Based Chiral Chemical Probes for Simultaneous Enantio- and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy
JournalChemistry - A European Journal
AuthorsShyshkanov, Sergey A.Author
Orlov, Nikolai V.Author
Year2016 (October 17)Volume22
Issue43
PublisherWiley
DOIdoi:10.1002/chem.201602884Search in ResearchGate
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Mindat Ref. ID8266276Long-form Identifiermindat:1:5:8266276:7
GUID0
Full ReferenceShyshkanov, Sergey A., Orlov, Nikolai V. (2016) Design of Selenium-Based Chiral Chemical Probes for Simultaneous Enantio- and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy. Chemistry - A European Journal, 22 (43). 15458-15467 doi:10.1002/chem.201602884
Plain TextShyshkanov, Sergey A., Orlov, Nikolai V. (2016) Design of Selenium-Based Chiral Chemical Probes for Simultaneous Enantio- and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy. Chemistry - A European Journal, 22 (43). 15458-15467 doi:10.1002/chem.201602884
In(2016, October) Chemistry - A European Journal Vol. 22 (43) Wiley

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Hamark, Christoffer, Landström, Jens, Widmalm, Göran (2014) SEAL by NMR: Glyco-Based Selenium-Labeled Affinity Ligands Detected by NMR Spectroscopy. Chemistry - A European Journal, 20 (43). 13905-13908 doi:10.1002/chem.201404933
Silva, Marcio S., Pietrobom, Daniel (2015) Chiral discrimination of β-telluride carboxylic acids by NMR spectroscopy. New Journal of Chemistry, 39. 8240-8244 doi:10.1039/c5nj01877c
Orlov, Nikolay V., Ananikov, Valentine P. (2010) First principles design of derivatizing agent for direct determination of enantiomeric purity of chiral alcohols and amines by NMR spectroscopy. Chemical Communications, 46 (18). 3212pp. doi:10.1039/b923359h
Ikeda, Ryuhei, Kuwano, Ryoichi (2016) Asymmetric Hydrogenation of Isoxazolium Triflates with a Chiral Iridium Catalyst. Chemistry - A European Journal, 22 (25). 8610-8618 doi:10.1002/chem.201600732
Eckert, Prisca K., Golz, Christopher, Degen, Patrick, Werner, Cornelia, Rehage, Heinz, Strohmann, Carsten (2014) Exploring the Synthesis of a New Group of Chiral Ammonium Salts with Specific Configurations at the Stereogenic Nitrogen Centers. Chemistry - A European Journal, 20 (12). 3268-3272 doi:10.1002/chem.201304433
Pham, Manh V., Cramer, Nicolai (2016) Enantioselective Access to Spirocyclic Sultams by Chiral Cpx -Rhodium(III)-Catalyzed Annulations. Chemistry - A European Journal, 22 (7). 2270-2273 doi:10.1002/chem.201504998
Adly, Frady G., Gardiner, Michael G., Ghanem, Ashraf (2016) Design and Synthesis of Novel Chiral Dirhodium(II) Carboxylate Complexes for Asymmetric Cyclopropanation Reactions. Chemistry - A European Journal, 22 (10). 3447-3461 doi:10.1002/chem.201504817
Granqvist, Lotta, Virta, Pasi (2016) Characterization of G-Quadruplex/Hairpin Transitions of RNAs by19F NMR Spectroscopy. Chemistry - A European Journal, 22 (43). 15360-15372 doi:10.1002/chem.201602898
Malinakova, Helena C. (2004) Chiral Nonracemic Late-Transition-Metal Organometallics with a Metal-Bonded Stereogenic Carbon Atom: Development of New Tools for Asymmetric Organic Synthesis. Chemistry - A European Journal, 10 (11). 2636-2646 doi:10.1002/chem.200305667
(2025) RETRACTION: NDI Based C2‐symmetric Chiral Supramolecular Hydrogels Towards Enhanced Conductivity. Chemistry – A European Journal, 31 (22). doi:10.1002/chem.202500777
Gangopadhyay, Monalisa, Maity, Arunava, Dey, Ananta, Rajamohanan, P. R., Ravindranathan, Sapna, Das, Amitava (2017) Chiral Discrimination through 1 H NMR and Luminescence Spectroscopy: Dynamic Processes and Solid Strip for Chiral Recognition. Chemistry - A European Journal, 23 (72). 18303-18313 doi:10.1002/chem.201704837
 
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