Artículos de revistas sobre el tema "Chiral Substrates"
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Matthews, Jermey N. A. "Shedding light on chiral substrates". Physics Today 64, n.º 11 (noviembre de 2011): 19. http://dx.doi.org/10.1063/pt.3.1320.
Texto completoCoscolín, Cristina, Mónica Martínez-Martínez, Jennifer Chow, Rafael Bargiela, Antonio García-Moyano, Gro Bjerga, Alexander Bollinger et al. "Relationships between Substrate Promiscuity and Chiral Selectivity of Esterases from Phylogenetically and Environmentally Diverse Microorganisms". Catalysts 8, n.º 1 (5 de enero de 2018): 10. http://dx.doi.org/10.3390/catal8010010.
Texto completoFerraccioli, Raffaella. "Progress on the Stereoselective Synthesis of Chiral Molecules Based on Metal-Catalyzed Dynamic Kinetic Resolution of Alcohols with Lipases". Symmetry 13, n.º 9 (19 de septiembre de 2021): 1744. http://dx.doi.org/10.3390/sym13091744.
Texto completoMu, Xiaojing, Xiaoqi Yi, Shangyou Xiao, Chengshan Wang, Gang Chen y Yan Li. "Substrates for Paraoxonase". Current Pharmaceutical Design 24, n.º 5 (2 de mayo de 2018): 615–27. http://dx.doi.org/10.2174/1381612824666171213102310.
Texto completoRecchimurzo, Alessandra, Federica Balzano, Gloria Uccello Barretta, Luca Gherardi, Milo Malanga y Federica Aiello. "Silylated-Acetylated Cyclodextrins as Chiral Sensors for the Enantiodiscrimination of Fluorinated Anesthetics". Molecules 28, n.º 6 (20 de marzo de 2023): 2804. http://dx.doi.org/10.3390/molecules28062804.
Texto completoBhaskararao, Bangaru y Raghavan B. Sunoj. "Two chiral catalysts in action: insights into cooperativity and stereoselectivity in proline and cinchona-thiourea dual organocatalysis". Chemical Science 9, n.º 46 (2018): 8738–47. http://dx.doi.org/10.1039/c8sc03078b.
Texto completoLibrizzi, Paulina, Aneek Biswas, Roger Chang, Xiang-Tian Kong, Matthew Moocarme, Gaurav Ahuja, Ilona Kretzschmar y Luat T. Vuong. "Broadband chiral hybrid plasmon modes on nanofingernail substrates". Nanoscale 12, n.º 6 (2020): 3827–33. http://dx.doi.org/10.1039/c9nr07394a.
Texto completoMüller, Christiane y Thorsten Bach. "Chirality Control in Photochemical Reactions: Enantioselective Formation of Complex Photoproducts in Solution". Australian Journal of Chemistry 61, n.º 8 (2008): 557. http://dx.doi.org/10.1071/ch08195.
Texto completoPozar, D. M. "Microstrip antennas and arrays on chiral substrates". IEEE Transactions on Antennas and Propagation 40, n.º 10 (1992): 1260–63. http://dx.doi.org/10.1109/8.182462.
Texto completoSukenik, Nir, Francesco Tassinari, Shira Yochelis, Oded Millo, Lech Tomasz Baczewski y Yossi Paltiel. "Correlation between Ferromagnetic Layer Easy Axis and the Tilt Angle of Self Assembled Chiral Molecules". Molecules 25, n.º 24 (20 de diciembre de 2020): 6036. http://dx.doi.org/10.3390/molecules25246036.
Texto completoMiyabe, Hideto, Ryuta Asada y Yoshiji Takemoto. "Cascade radical reaction of substrates with a carbon–carbon triple bond as a radical acceptor". Beilstein Journal of Organic Chemistry 9 (13 de junio de 2013): 1148–55. http://dx.doi.org/10.3762/bjoc.9.128.
Texto completoKlyuev, Dmitriy, Anatoly Neshcheret, Oleg Osipov y Aleksandr Potapov. "Mathematical Modeling of Multi-Element Antenna Arrays with Chiral Metamaterials Substrates Using Singular Integral Equations". EPJ Web of Conferences 224 (2019): 02002. http://dx.doi.org/10.1051/epjconf/201922402002.
Texto completoБузова, М. А., Д. С. Клюев, М. А. Минкин, А. М. Нещерет y Ю. В. Соколова. "Решение электродинамической задачи для микрополосковой излучающей структуры с киральной подложкой". Письма в журнал технической физики 44, n.º 11 (2018): 80. http://dx.doi.org/10.21883/pjtf.2018.11.46200.17147.
Texto completoKamlar, Martin, Jan Vesely y Ramon Rios Torres. "ChemInform Abstract: Diastereoselective Pauson-Khand Reaction Using Chiral Pool Techniques (Chiral Substrates)". ChemInform 44, n.º 18 (11 de abril de 2013): no. http://dx.doi.org/10.1002/chin.201318269.
Texto completoXue, Ya-Ping, Cheng-Hao Cao y Yu-Guo Zheng. "Enzymatic asymmetric synthesis of chiral amino acids". Chemical Society Reviews 47, n.º 4 (2018): 1516–61. http://dx.doi.org/10.1039/c7cs00253j.
Texto completoTrushin O.S., Fattakhov I.S., Popov A.A., Mazaletsky L.A., Lomov A.A., Zakharov D.M., Gaidukasov R.A., Miakonkikh A.V. y Shendrikova L.A. "Tailoring magnetic anisotropy and optical characteristics of nanostructural Co films by oblique angle deposition". Physics of the Solid State 65, n.º 6 (2023): 953. http://dx.doi.org/10.21883/pss.2023.06.56107.16h.
Texto completoAdamčíková, Ľubica, Katarína Kučárová y Peter Ševčík. "The Belousov-Zhabotinskii Oscillatory Reaction Involving Some Organic Chiral Substrates". Collection of Czechoslovak Chemical Communications 62, n.º 5 (1997): 739–45. http://dx.doi.org/10.1135/cccc19970739.
Texto completoMiyaji, Ryota, Yuuki Wada, Akira Matsumoto, Keisuke Asano y Seijiro Matsubara. "Bifunctional organocatalysts for the asymmetric synthesis of axially chiral benzamides". Beilstein Journal of Organic Chemistry 13 (2 de agosto de 2017): 1518–23. http://dx.doi.org/10.3762/bjoc.13.151.
Texto completoIto, Hajime, Shinichiro Ito, Yusuke Sasaki, Kou Matsuura y Masaya Sawamura. "Copper-catalyzed substitution of allylic carbonates with diboron: A new approach to allylboronate synthesis". Pure and Applied Chemistry 80, n.º 5 (1 de enero de 2008): 1039–45. http://dx.doi.org/10.1351/pac200880051039.
Texto completoCetin, Adnan. "Chiral Catalysts Utilized in the Nucleophilic Addition of Dialkyl-zinc Reagents to Carbonyl Compounds". Letters in Organic Chemistry 17, n.º 8 (18 de agosto de 2020): 571–85. http://dx.doi.org/10.2174/1570178617666191220145038.
Texto completoBasavaiah, D., V. V. L. Gowriswari, P. K. S. Sarma y P. Dharma Rao. "Chiral acrylates as substrates in baylis-hillman reaction". Tetrahedron Letters 31, n.º 11 (enero de 1990): 1621–24. http://dx.doi.org/10.1016/0040-4039(90)80033-i.
Texto completoSheng, X. Q. y E. K. N. Yung. "Analysis of microstrip antennas on finite chiral substrates". International Journal of RF and Microwave Computer-Aided Engineering 14, n.º 1 (2003): 49–56. http://dx.doi.org/10.1002/mmce.10115.
Texto completoZhang, Mingliang, Victor Pacheco-Peña, Yao Yu, Wenxiang Chen, Nicholas J. Greybush, Aaron Stein, Nader Engheta, Christopher B. Murray y Cherie R. Kagan. "Nanoimprinted Chiral Plasmonic Substrates with Three-Dimensional Nanostructures". Nano Letters 18, n.º 11 (26 de septiembre de 2018): 7389–94. http://dx.doi.org/10.1021/acs.nanolett.8b03785.
Texto completoBakonyi, Daniel, Christine Toelzer, Michael Stricker, Werner Hummel, Karsten Niefind y Harald Gröger. "Expanding the Application Range of Microbial Oxidoreductases by an Alcohol Dehydrogenase from Comamonas testosteroni with a Broad Substrate Spectrum and pH Profile". Catalysts 10, n.º 11 (4 de noviembre de 2020): 1281. http://dx.doi.org/10.3390/catal10111281.
Texto completoAdam, M., C. Damblon, B. Plaitin, L. Christiaens y J. M. Frère. "Chromogenic depsipeptide substrates for β-lactamases and penicillin-sensitive dd-peptidases". Biochemical Journal 270, n.º 2 (1 de septiembre de 1990): 525–29. http://dx.doi.org/10.1042/bj2700525.
Texto completoJain, Nilesh, Ravi B. Patel y Ashutosh V. Bedekar. "Modified Kagan's amide: synthesis and application as a chiral solvating agent for hydrogen-bonding based chiral discrimination in NMR". RSC Advances 5, n.º 57 (2015): 45943–55. http://dx.doi.org/10.1039/c5ra06959a.
Texto completoRíos, Pablo, Tiddo J. Mooibroek, Tom S. Carter, Christopher Williams, Miriam R. Wilson, Matthew P. Crump y Anthony P. Davis. "Enantioselective carbohydrate recognition by synthetic lectins in water". Chemical Science 8, n.º 5 (2017): 4056–61. http://dx.doi.org/10.1039/c6sc05399h.
Texto completoZgorzelak, Mikołaj, Jakub Grajewski, Jacek Gawroński y Marcin Kwit. "Solvent-assisted synthesis of a shape-persistent chiral polyaza gigantocycle characterized by a very large internal cavity and extraordinarily high amplitude of the ECD exciton couplet". Chemical Communications 55, n.º 16 (2019): 2301–4. http://dx.doi.org/10.1039/c8cc10184a.
Texto completoVerpaalen, Rob C. P., Michael G. Debije, Cees W. M. Bastiaansen, Haris Halilović, Tom A. P. Engels y Albertus P. H. J. Schenning. "Programmable helical twisting in oriented humidity-responsive bilayer films generated by spray-coating of a chiral nematic liquid crystal". Journal of Materials Chemistry A 6, n.º 36 (2018): 17724–29. http://dx.doi.org/10.1039/c8ta06984k.
Texto completoHolland, Herbert L., Carl D. Turner, Peter R. Andreana y Doan Nguyen. "Article". Canadian Journal of Chemistry 77, n.º 4 (1 de abril de 1999): 463–71. http://dx.doi.org/10.1139/v99-068.
Texto completoMorrison, D. J., J. M. Blackwell y W. E. Piers. "Mechanistic insights into perfluoroaryl borane-catalyzed allylstannations: Toward asymmetric induction with chiral boranes". Pure and Applied Chemistry 76, n.º 3 (1 de enero de 2004): 615–23. http://dx.doi.org/10.1351/pac200476030615.
Texto completoMerelli, Bérangère, Laurence Menguy, Estelle Soubeyrand-Lenoir y Jean-Claude Cherton. "Determination of the enantiomeric composition of chiral delta-2-thiazolines-1,3 by1H and19F NMR spectroscopy using chiral solvating agents". Spectroscopy 20, n.º 3 (2006): 95–107. http://dx.doi.org/10.1155/2006/698685.
Texto completoHan, Jung Tae, Jin Yong Lee y Jaesook Yun. "Asymmetric synthesis of γ-chiral borylalkanes via sequential reduction/hydroboration using a single copper catalyst". Chemical Science 11, n.º 33 (2020): 8961–65. http://dx.doi.org/10.1039/d0sc03759a.
Texto completoMimura, Shohei, Sho Mizushima, Yohei Shimizu y Masaya Sawamura. "Copper-catalyzed enantioselective conjugate reduction of α,β-unsaturated esters with chiral phenol–carbene ligands". Beilstein Journal of Organic Chemistry 16 (31 de marzo de 2020): 537–43. http://dx.doi.org/10.3762/bjoc.16.50.
Texto completoSoundararajan, Karthikeyan, Helen Ratna Monica Jeyarajan, Raju Subimol Kamarajapurathu y Karthik Krishna Kumar Ayyanoth. "Facile and innovative catalytic protocol for intramolecular Friedel–Crafts cyclization of Morita–Baylis–Hillman adducts: Synergistic combination of chiral (salen)chromium(III)/BF3·OEt2 catalysis". Beilstein Journal of Organic Chemistry 17 (26 de agosto de 2021): 2186–93. http://dx.doi.org/10.3762/bjoc.17.140.
Texto completoRamachary, Dhevalapally B. y Kodambahalli S. Shruthi. "Asymmetric synthesis of tetrahydroquinolines through supramolecular organocatalysis". Org. Biomol. Chem. 12, n.º 25 (2014): 4300–4304. http://dx.doi.org/10.1039/c4ob00570h.
Texto completoUemura, Naohiro, Seiya Toyoda, Waku Shimizu, Yasushi Yoshida, Takashi Mino y Masami Sakamoto. "Absolute Asymmetric Synthesis Involving Chiral Symmetry Breaking in Diels–Alder Reaction". Symmetry 12, n.º 6 (1 de junio de 2020): 910. http://dx.doi.org/10.3390/sym12060910.
Texto completoBanerjee-Ghosh, Koyel, Oren Ben Dor, Francesco Tassinari, Eyal Capua, Shira Yochelis, Amir Capua, See-Hun Yang et al. "Separation of enantiomers by their enantiospecific interaction with achiral magnetic substrates". Science 360, n.º 6395 (10 de mayo de 2018): 1331–34. http://dx.doi.org/10.1126/science.aar4265.
Texto completoPuentes, Cira Mollings y Thomas J. Wenzel. "Phosphated cyclodextrins as water-soluble chiral NMR solvating agents for cationic compounds". Beilstein Journal of Organic Chemistry 13 (6 de enero de 2017): 43–53. http://dx.doi.org/10.3762/bjoc.13.6.
Texto completoZhang, Qingfeng, Taylor Hernandez, Kyle W. Smith, Seyyed Ali Hosseini Jebeli, Alan X. Dai, Lauren Warning, Rashad Baiyasi et al. "Unraveling the origin of chirality from plasmonic nanoparticle-protein complexes". Science 365, n.º 6460 (26 de septiembre de 2019): 1475–78. http://dx.doi.org/10.1126/science.aax5415.
Texto completoHong, Suk-Bong y Frank M. Raushel. "Stereochemical preferences for chiral substrates by the bacterial phosphotriesterase". Chemico-Biological Interactions 119-120 (mayo de 1999): 225–34. http://dx.doi.org/10.1016/s0009-2797(99)00031-9.
Texto completoYadav, J. S. y S. Nanda. "Novel chiral lipoxygenase substrates: design and synthesis. Part 2". Tetrahedron: Asymmetry 12, n.º 23 (diciembre de 2001): 3223–34. http://dx.doi.org/10.1016/s0957-4166(02)00009-5.
Texto completoMurphy, James P., Mark Nieuwenhuyzen, Karen Reynolds, Pakala K. S. Sarma y Paul J. Stevenson. "Chiral dienamides- substrates for asymmetric synthesis of amido cyclohexenes". Tetrahedron Letters 36, n.º 52 (diciembre de 1995): 9533–36. http://dx.doi.org/10.1016/0040-4039(95)02040-3.
Texto completoMumtaz, Salma, Israel Cano, Nargis Mumtaz, Ahmed Abbas, Jairton Dupont y Humaira Yasmeen Gondal. "Supramolecular interaction of non-racemic benzimidazolium based ion pairs with chiral substrates". Physical Chemistry Chemical Physics 20, n.º 32 (2018): 20821–26. http://dx.doi.org/10.1039/c8cp03881c.
Texto completoZhou, Huan, Wenlei Zhao, Tao Zhang, Haodong Guo, Haizhou Huang y Mingxin Chang. "Enantioselective Synthesis of 2-Substituted Pyrrolidines via Intramolecular Reductive Amination". Synthesis 51, n.º 13 (7 de mayo de 2019): 2713–19. http://dx.doi.org/10.1055/s-0037-1611533.
Texto completoMetallinos, Costa, Ngan Tran y Dusty Cadwallader. "Diastereoselective Synthesis of Alkylated 1,4-Cyclohexadiene Esters Using Epimeric Pyrroloimidazolones". Synthesis 53, n.º 01 (24 de agosto de 2020): 182–92. http://dx.doi.org/10.1055/s-0040-1707351.
Texto completoZhang, Yue Cheng, Jing Yuan Gao, Nai Yue Shi y Ji Quan Zhao. "Synthesis of Chiral Tridentate Ligands Embodying the Bispidine Framework and their Application in the Enantioselective Addition of Diethylzinc to Aldehydes". Advanced Materials Research 396-398 (noviembre de 2011): 1236–43. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.1236.
Texto completoThomas, Fabian, Dominik Steden, Alexander Eith, Alexander Hoffmann y Sonja Herres-Pawlis. "Chiral bis(pyrazolyl)methane copper(I) complexes and their application in nitrene transfer reactions". Zeitschrift für Naturforschung B 76, n.º 10-12 (29 de octubre de 2021): 835–47. http://dx.doi.org/10.1515/znb-2021-0140.
Texto completoWu, Xianqing, Mohini Shrestha y Yifeng Chen. "Asymmetric Synthesis of α-Alkylated γ-Lactam via Nickel/8-Quinim-Catalyzed Reductive Alkyl-Carbamoylation of Unactivated Alkene". Synlett 32, n.º 10 (14 de enero de 2021): 955–61. http://dx.doi.org/10.1055/a-1353-7605.
Texto completoMakino, Yoshihide, Kousuke Inoue, Tohru Dairi y Nobuya Itoh. "Engineering of Phenylacetaldehyde Reductase for Efficient Substrate Conversion in Concentrated 2-Propanol". Applied and Environmental Microbiology 71, n.º 8 (agosto de 2005): 4713–20. http://dx.doi.org/10.1128/aem.71.8.4713-4720.2005.
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