Статті в журналах з теми "Late stage fluorination"
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Tang, Pingping, Takeru Furuya, and Tobias Ritter. "Silver-Catalyzed Late-Stage Fluorination." Journal of the American Chemical Society 132, no. 34 (September 2010): 12150–54. http://dx.doi.org/10.1021/ja105834t.
Повний текст джерелаCampbell, Michael G., and Tobias Ritter. "Late-Stage Fluorination: From Fundamentals to Application." Organic Process Research & Development 18, no. 4 (March 11, 2014): 474–80. http://dx.doi.org/10.1021/op400349g.
Повний текст джерелаAbele, Stefan, and Hans-Jürgen Federsel. "Invited Academic Review on Late-Stage Fluorination." Organic Process Research & Development 18, no. 4 (March 11, 2014): 473. http://dx.doi.org/10.1021/op5000539.
Повний текст джерелаBrooks, Allen F., Joseph J. Topczewski, Naoko Ichiishi, Melanie S. Sanford, and Peter J. H. Scott. "Late-stage [18F]fluorination: new solutions to old problems." Chem. Sci. 5, no. 12 (2014): 4545–53. http://dx.doi.org/10.1039/c4sc02099e.
Повний текст джерелаWu, Qiuzi, Yang-Jie Mao, Kun Zhou, Shuang Wang, Lei Chen, Zhen-Yuan Xu, Shao-Jie Lou, and Dan-Qian Xu. "Pd-Catalysed direct C(sp2)–H fluorination of aromatic ketones: concise access to anacetrapib." Chemical Communications 57, no. 37 (2021): 4544–47. http://dx.doi.org/10.1039/d1cc01047f.
Повний текст джерелаNeumann, Constanze N., and Tobias Ritter. "Late-Stage Fluorination: Fancy Novelty or Useful Tool?" Angewandte Chemie International Edition 54, no. 11 (February 4, 2015): 3216–21. http://dx.doi.org/10.1002/anie.201410288.
Повний текст джерелаCampbell, Michael G., and Tobias Ritter. "ChemInform Abstract: Late-Stage Fluorination: From Fundamentals to Application." ChemInform 45, no. 25 (June 5, 2014): no. http://dx.doi.org/10.1002/chin.201425239.
Повний текст джерелаYerien, Damian E., Sergio Bonesi, and Al Postigo. "Fluorination methods in drug discovery." Organic & Biomolecular Chemistry 14, no. 36 (2016): 8398–427. http://dx.doi.org/10.1039/c6ob00764c.
Повний текст джерелаNeumann, Constanze N., and Tobias Ritter. "ChemInform Abstract: Late-Stage Fluorination: Fancy Novelty or Useful Tool?" ChemInform 46, no. 19 (April 23, 2015): no. http://dx.doi.org/10.1002/chin.201519317.
Повний текст джерелаS. Clemente, Gonçalo, Tryfon Zarganes-Tzitzikas, Alexander Dömling, and Philip H. Elsinga. "Late-Stage Copper-Catalyzed Radiofluorination of an Arylboronic Ester Derivative of Atorvastatin." Molecules 24, no. 23 (November 20, 2019): 4210. http://dx.doi.org/10.3390/molecules24234210.
Повний текст джерелаBalandeh, Mehrdad, and Saman Sadeghi. "(Invited) Fluorination and No-Carrier-Added Radio-Fluorination of Organic Molecules Using Cation Pool Technique." ECS Meeting Abstracts MA2022-02, no. 30 (October 9, 2022): 1111. http://dx.doi.org/10.1149/ma2022-02301111mtgabs.
Повний текст джерелаBritton, Robert, and Michael Meanwell. "Synthesis of Heterobenzylic Fluorides." Synthesis 50, no. 06 (January 23, 2018): 1228–36. http://dx.doi.org/10.1055/s-0036-1589159.
Повний текст джерелаLee, E., A. S. Kamlet, D. C. Powers, C. N. Neumann, G. B. Boursalian, T. Furuya, D. C. Choi, J. M. Hooker, and T. Ritter. "A Fluoride-Derived Electrophilic Late-Stage Fluorination Reagent for PET Imaging." Science 334, no. 6056 (November 3, 2011): 639–42. http://dx.doi.org/10.1126/science.1212625.
Повний текст джерелаBrooks, Allen F., Joseph J. Topczewski, Naoko Ichiishi, Melanie S. Sanford, and Peter J. H. Scott. "ChemInform Abstract: Late-Stage [18F]Fluorination: New Solutions to Old Problems." ChemInform 45, no. 52 (December 11, 2014): no. http://dx.doi.org/10.1002/chin.201452263.
Повний текст джерелаStewart, Megan N., Brian G. Hockley, and Peter J. H. Scott. "Green approaches to late-stage fluorination: radiosyntheses of 18F-labelled radiopharmaceuticals in ethanol and water." Chemical Communications 51, no. 79 (2015): 14805–8. http://dx.doi.org/10.1039/c5cc05919d.
Повний текст джерелаJakobsson, Jimmy Erik, and Patrick Johannes Riss. "Transition metal free, late-stage, regiospecific, aromatic fluorination on a preparative scale using a KF/crypt-222 complex." RSC Advances 8, no. 38 (2018): 21288–91. http://dx.doi.org/10.1039/c8ra03757d.
Повний текст джерелаCole, Erin, Megan Stewart, Ryan Littich, Raphael Hoareau, and Peter Scott. "Radiosyntheses using Fluorine-18: The Art and Science of Late Stage Fluorination." Current Topics in Medicinal Chemistry 14, no. 7 (March 31, 2014): 875–900. http://dx.doi.org/10.2174/1568026614666140202205035.
Повний текст джерелаHuang, Xiongyi, Wei Liu, Hong Ren, Ramesh Neelamegam, Jacob M. Hooker, and John T. Groves. "Late Stage Benzylic C–H Fluorination with [18F]Fluoride for PET Imaging." Journal of the American Chemical Society 136, no. 19 (May 6, 2014): 6842–45. http://dx.doi.org/10.1021/ja5039819.
Повний текст джерелаLi, Jiakun, Junting Chen, Ruocheng Sang, Won-Seok Ham, Matthew B. Plutschack, Florian Berger, Sonia Chabbra, Alexander Schnegg, Christophe Genicot, and Tobias Ritter. "Photoredox catalysis with aryl sulfonium salts enables site-selective late-stage fluorination." Nature Chemistry 12, no. 1 (November 25, 2019): 56–62. http://dx.doi.org/10.1038/s41557-019-0353-3.
Повний текст джерелаXu, Peng, Da Zhao, Florian Berger, Aboubakr Hamad, Jens Rickmeier, Roland Petzold, Mykhailo Kondratiuk, Kostiantyn Bohdan, and Tobias Ritter. "Site‐Selective Late‐Stage Aromatic [ 18 F]Fluorination via Aryl Sulfonium Salts." Angewandte Chemie 132, no. 5 (December 12, 2019): 1972–76. http://dx.doi.org/10.1002/ange.201912567.
Повний текст джерелаBermejo Góme, Antonio, Miguel A. Cortés González, Marvin Lübcke, Magnus J. Johansson, Magnus Schou, and Kálmán J. Szabó. "Synthesis of trifluoromethyl moieties by late-stage copper (I) mediated nucleophilic fluorination." Journal of Fluorine Chemistry 194 (February 2017): 51–57. http://dx.doi.org/10.1016/j.jfluchem.2016.12.017.
Повний текст джерелаXu, Peng, Da Zhao, Florian Berger, Aboubakr Hamad, Jens Rickmeier, Roland Petzold, Mykhailo Kondratiuk, Kostiantyn Bohdan, and Tobias Ritter. "Site‐Selective Late‐Stage Aromatic [ 18 F]Fluorination via Aryl Sulfonium Salts." Angewandte Chemie International Edition 59, no. 5 (January 27, 2020): 1956–60. http://dx.doi.org/10.1002/anie.201912567.
Повний текст джерелаFanelli, Roberto, Florine Cavelier та Jean Martinez. "Expedient Synthesis of Fmoc-(S)-γ-Fluoroleucine and Late-Stage Fluorination of Peptides". Synlett 27, № 09 (16 лютого 2016): 1403–7. http://dx.doi.org/10.1055/s-0035-1561568.
Повний текст джерелаMeanwell, Michael, Matthew B. Nodwell, Rainer E. Martin, and Robert Britton. "A Convenient Late-Stage Fluorination of Pyridylic C−H Bonds with N -Fluorobenzenesulfonimide." Angewandte Chemie International Edition 55, no. 42 (October 6, 2016): 13244–48. http://dx.doi.org/10.1002/anie.201606323.
Повний текст джерелаMeanwell, Michael, Matthew B. Nodwell, Rainer E. Martin, and Robert Britton. "A Convenient Late-Stage Fluorination of Pyridylic C−H Bonds with N -Fluorobenzenesulfonimide." Angewandte Chemie 128, no. 42 (October 6, 2016): 13438–42. http://dx.doi.org/10.1002/ange.201606323.
Повний текст джерелаLou, Shao-Jie, Qi Chen, Yi-Feng Wang, Dan-Qian Xu, Xiao-Hua Du, Jiang-Qi He, Yang-Jie Mao, and Zhen-Yuan Xu. "Selective C–H Bond Fluorination of Phenols with a Removable Directing Group: Late-Stage Fluorination of 2-Phenoxyl Nicotinate Derivatives." ACS Catalysis 5, no. 5 (April 2015): 2846–49. http://dx.doi.org/10.1021/acscatal.5b00306.
Повний текст джерелаCole, Erin L., Megan N. Stewart, Ryan Littich, Raphael Hoareau, and Peter J. H. Scott. "ChemInform Abstract: Radiosyntheses Using Fluorine-18: The Art and Science of Late Stage Fluorination." ChemInform 45, no. 41 (September 25, 2014): no. http://dx.doi.org/10.1002/chin.201441273.
Повний текст джерелаFier, Patrick S., and John F. Hartwig. "Synthesis and Late-Stage Functionalization of Complex Molecules through C–H Fluorination and Nucleophilic Aromatic Substitution." Journal of the American Chemical Society 136, no. 28 (July 2014): 10139–47. http://dx.doi.org/10.1021/ja5049303.
Повний текст джерелаCavaliere, Alessandra, Katrin C. Probst, Stephen J. Paisey, Christopher Marshall, Abdul K. H. Dheere, Franklin Aigbirhio, Christopher McGuigan, and Andrew D. Westwell. "Radiosynthesis of [18F]-Labelled Pro-Nucleotides (ProTides)." Molecules 25, no. 3 (February 6, 2020): 704. http://dx.doi.org/10.3390/molecules25030704.
Повний текст джерелаCraig, Austin, Niklas Kolks, Elizaveta A. Urusova, Johannes Zischler, Melanie Brugger, Heike Endepols, Bernd Neumaier, and Boris D. Zlatopolskiy. "Preparation of labeled aromatic amino acids via late-stage 18F-fluorination of chiral nickel and copper complexes." Chemical Communications 56, no. 66 (2020): 9505–8. http://dx.doi.org/10.1039/d0cc02223c.
Повний текст джерелаYuan, Zheliang, Matthew B. Nodwell, Hua Yang, Noeen Malik, Helen Merkens, François Bénard, Rainer E. Martin, Paul Schaffer, and Robert Britton. "Site-Selective, Late-Stage C−H 18 F-Fluorination on Unprotected Peptides for Positron Emission Tomography Imaging." Angewandte Chemie 130, no. 39 (September 5, 2018): 12915–18. http://dx.doi.org/10.1002/ange.201806966.
Повний текст джерелаYuan, Zheliang, Matthew B. Nodwell, Hua Yang, Noeen Malik, Helen Merkens, François Bénard, Rainer E. Martin, Paul Schaffer, and Robert Britton. "Site-Selective, Late-Stage C−H 18 F-Fluorination on Unprotected Peptides for Positron Emission Tomography Imaging." Angewandte Chemie International Edition 57, no. 39 (September 5, 2018): 12733–36. http://dx.doi.org/10.1002/anie.201806966.
Повний текст джерелаFier, Patrick S., and John F. Hartwig. "ChemInform Abstract: Synthesis and Late-Stage Functionalization of Complex Molecules Through C-H Fluorination and Nucleophilic Aromatic Substitution." ChemInform 46, no. 7 (January 29, 2015): no. http://dx.doi.org/10.1002/chin.201507242.
Повний текст джерелаAbularrage, Nile S., Brian J. Levandowski, and Ronald T. Raines. "Synthesis and Diels–Alder Reactivity of 4-Fluoro-4-Methyl-4H-Pyrazoles." International Journal of Molecular Sciences 21, no. 11 (May 31, 2020): 3964. http://dx.doi.org/10.3390/ijms21113964.
Повний текст джерелаPromontorio, Rossella, Jean-Alexandre Richard, and Charles M. Marson. "Late-stage fluorination of bridged scaffolds: Chemoselective generation of a CHF group at three positions of the bicyclo[3.3.1]nonane system." Tetrahedron Letters 59, no. 13 (March 2018): 1226–29. http://dx.doi.org/10.1016/j.tetlet.2018.02.038.
Повний текст джерелаScroggie, Kymberley R., Lisa J. Alcock, Maria J. Matos, Gonçalo J. L. Bernardes, Michael V. Perkins, and Justin M. Chalker. "A silicon-labelled amino acid suitable for late-stage fluorination and unexpected oxidative cleavage reactions in the preparation of a key intermediate in the Strecker synthesis." Peptide Science 110, no. 3 (April 20, 2018): e24069. http://dx.doi.org/10.1002/pep2.24069.
Повний текст джерела"Copper-Mediated Late-Stage Fluorination of Arenes Using Photoredox Catalysis." Synfacts 16, no. 02 (January 21, 2020): 0163. http://dx.doi.org/10.1055/s-0039-1691473.
Повний текст джерелаAjenjo, Javier, Gianluca Destro, Bart Cornelissen, and Véronique Gouverneur. "Closing the gap between 19F and 18F chemistry." EJNMMI Radiopharmacy and Chemistry 6, no. 1 (September 25, 2021). http://dx.doi.org/10.1186/s41181-021-00143-y.
Повний текст джерелаChang, Zhe, Jialin Huang, Si Wang, Geshuyi Chen, Heng Zhao, Rui Wang, and Depeng Zhao. "Copper catalyzed late-stage C(sp3)-H functionalization of nitrogen heterocycles." Nature Communications 12, no. 1 (July 15, 2021). http://dx.doi.org/10.1038/s41467-021-24671-y.
Повний текст джерелаKim, Jeongmin, Changkun Park, Keewook Yi, Shinae Lee, Sook Ju Kim, Min-Ji Jung, and Albert Chang-sik Cheong. "COM-1 and Hongcheon: New monazite reference materials for the microspot analysis of oxygen isotopic composition." Journal of Analytical Science and Technology 13, no. 1 (October 4, 2022). http://dx.doi.org/10.1186/s40543-022-00342-5.
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