Статті в журналах з теми "Chiral Substrates"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Chiral Substrates".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Matthews, Jermey N. A. "Shedding light on chiral substrates." Physics Today 64, no. 11 (November 2011): 19. http://dx.doi.org/10.1063/pt.3.1320.
Повний текст джерелаCoscolín, 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, no. 1 (January 5, 2018): 10. http://dx.doi.org/10.3390/catal8010010.
Повний текст джерелаFerraccioli, Raffaella. "Progress on the Stereoselective Synthesis of Chiral Molecules Based on Metal-Catalyzed Dynamic Kinetic Resolution of Alcohols with Lipases." Symmetry 13, no. 9 (September 19, 2021): 1744. http://dx.doi.org/10.3390/sym13091744.
Повний текст джерелаMu, Xiaojing, Xiaoqi Yi, Shangyou Xiao, Chengshan Wang, Gang Chen, and Yan Li. "Substrates for Paraoxonase." Current Pharmaceutical Design 24, no. 5 (May 2, 2018): 615–27. http://dx.doi.org/10.2174/1381612824666171213102310.
Повний текст джерелаRecchimurzo, Alessandra, Federica Balzano, Gloria Uccello Barretta, Luca Gherardi, Milo Malanga, and Federica Aiello. "Silylated-Acetylated Cyclodextrins as Chiral Sensors for the Enantiodiscrimination of Fluorinated Anesthetics." Molecules 28, no. 6 (March 20, 2023): 2804. http://dx.doi.org/10.3390/molecules28062804.
Повний текст джерелаBhaskararao, Bangaru, and Raghavan B. Sunoj. "Two chiral catalysts in action: insights into cooperativity and stereoselectivity in proline and cinchona-thiourea dual organocatalysis." Chemical Science 9, no. 46 (2018): 8738–47. http://dx.doi.org/10.1039/c8sc03078b.
Повний текст джерелаLibrizzi, Paulina, Aneek Biswas, Roger Chang, Xiang-Tian Kong, Matthew Moocarme, Gaurav Ahuja, Ilona Kretzschmar, and Luat T. Vuong. "Broadband chiral hybrid plasmon modes on nanofingernail substrates." Nanoscale 12, no. 6 (2020): 3827–33. http://dx.doi.org/10.1039/c9nr07394a.
Повний текст джерелаMüller, Christiane, and Thorsten Bach. "Chirality Control in Photochemical Reactions: Enantioselective Formation of Complex Photoproducts in Solution." Australian Journal of Chemistry 61, no. 8 (2008): 557. http://dx.doi.org/10.1071/ch08195.
Повний текст джерелаPozar, D. M. "Microstrip antennas and arrays on chiral substrates." IEEE Transactions on Antennas and Propagation 40, no. 10 (1992): 1260–63. http://dx.doi.org/10.1109/8.182462.
Повний текст джерелаSukenik, Nir, Francesco Tassinari, Shira Yochelis, Oded Millo, Lech Tomasz Baczewski, and Yossi Paltiel. "Correlation between Ferromagnetic Layer Easy Axis and the Tilt Angle of Self Assembled Chiral Molecules." Molecules 25, no. 24 (December 20, 2020): 6036. http://dx.doi.org/10.3390/molecules25246036.
Повний текст джерелаMiyabe, Hideto, Ryuta Asada, and Yoshiji Takemoto. "Cascade radical reaction of substrates with a carbon–carbon triple bond as a radical acceptor." Beilstein Journal of Organic Chemistry 9 (June 13, 2013): 1148–55. http://dx.doi.org/10.3762/bjoc.9.128.
Повний текст джерелаKlyuev, Dmitriy, Anatoly Neshcheret, Oleg Osipov, and 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.
Повний текст джерелаБузова, М. А., Д. С. Клюев, М. А. Минкин, А. М. Нещерет та Ю. В. Соколова. "Решение электродинамической задачи для микрополосковой излучающей структуры с киральной подложкой". Письма в журнал технической физики 44, № 11 (2018): 80. http://dx.doi.org/10.21883/pjtf.2018.11.46200.17147.
Повний текст джерелаKamlar, Martin, Jan Vesely, and Ramon Rios Torres. "ChemInform Abstract: Diastereoselective Pauson-Khand Reaction Using Chiral Pool Techniques (Chiral Substrates)." ChemInform 44, no. 18 (April 11, 2013): no. http://dx.doi.org/10.1002/chin.201318269.
Повний текст джерелаXue, Ya-Ping, Cheng-Hao Cao, and Yu-Guo Zheng. "Enzymatic asymmetric synthesis of chiral amino acids." Chemical Society Reviews 47, no. 4 (2018): 1516–61. http://dx.doi.org/10.1039/c7cs00253j.
Повний текст джерелаTrushin O.S., Fattakhov I.S., Popov A.A., Mazaletsky L.A., Lomov A.A., Zakharov D.M., Gaidukasov R.A., Miakonkikh A.V., and Shendrikova L.A. "Tailoring magnetic anisotropy and optical characteristics of nanostructural Co films by oblique angle deposition." Physics of the Solid State 65, no. 6 (2023): 953. http://dx.doi.org/10.21883/pss.2023.06.56107.16h.
Повний текст джерелаAdamčíková, Ľubica, Katarína Kučárová, and Peter Ševčík. "The Belousov-Zhabotinskii Oscillatory Reaction Involving Some Organic Chiral Substrates." Collection of Czechoslovak Chemical Communications 62, no. 5 (1997): 739–45. http://dx.doi.org/10.1135/cccc19970739.
Повний текст джерелаMiyaji, Ryota, Yuuki Wada, Akira Matsumoto, Keisuke Asano, and Seijiro Matsubara. "Bifunctional organocatalysts for the asymmetric synthesis of axially chiral benzamides." Beilstein Journal of Organic Chemistry 13 (August 2, 2017): 1518–23. http://dx.doi.org/10.3762/bjoc.13.151.
Повний текст джерелаIto, Hajime, Shinichiro Ito, Yusuke Sasaki, Kou Matsuura, and Masaya Sawamura. "Copper-catalyzed substitution of allylic carbonates with diboron: A new approach to allylboronate synthesis." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 1039–45. http://dx.doi.org/10.1351/pac200880051039.
Повний текст джерелаCetin, Adnan. "Chiral Catalysts Utilized in the Nucleophilic Addition of Dialkyl-zinc Reagents to Carbonyl Compounds." Letters in Organic Chemistry 17, no. 8 (August 18, 2020): 571–85. http://dx.doi.org/10.2174/1570178617666191220145038.
Повний текст джерелаBasavaiah, D., V. V. L. Gowriswari, P. K. S. Sarma, and P. Dharma Rao. "Chiral acrylates as substrates in baylis-hillman reaction." Tetrahedron Letters 31, no. 11 (January 1990): 1621–24. http://dx.doi.org/10.1016/0040-4039(90)80033-i.
Повний текст джерелаSheng, X. Q., and E. K. N. Yung. "Analysis of microstrip antennas on finite chiral substrates." International Journal of RF and Microwave Computer-Aided Engineering 14, no. 1 (2003): 49–56. http://dx.doi.org/10.1002/mmce.10115.
Повний текст джерелаZhang, Mingliang, Victor Pacheco-Peña, Yao Yu, Wenxiang Chen, Nicholas J. Greybush, Aaron Stein, Nader Engheta, Christopher B. Murray, and Cherie R. Kagan. "Nanoimprinted Chiral Plasmonic Substrates with Three-Dimensional Nanostructures." Nano Letters 18, no. 11 (September 26, 2018): 7389–94. http://dx.doi.org/10.1021/acs.nanolett.8b03785.
Повний текст джерелаBakonyi, Daniel, Christine Toelzer, Michael Stricker, Werner Hummel, Karsten Niefind, and 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, no. 11 (November 4, 2020): 1281. http://dx.doi.org/10.3390/catal10111281.
Повний текст джерелаAdam, M., C. Damblon, B. Plaitin, L. Christiaens та J. M. Frère. "Chromogenic depsipeptide substrates for β-lactamases and penicillin-sensitive dd-peptidases". Biochemical Journal 270, № 2 (1 вересня 1990): 525–29. http://dx.doi.org/10.1042/bj2700525.
Повний текст джерелаJain, Nilesh, Ravi B. Patel, and 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, no. 57 (2015): 45943–55. http://dx.doi.org/10.1039/c5ra06959a.
Повний текст джерелаRíos, Pablo, Tiddo J. Mooibroek, Tom S. Carter, Christopher Williams, Miriam R. Wilson, Matthew P. Crump, and Anthony P. Davis. "Enantioselective carbohydrate recognition by synthetic lectins in water." Chemical Science 8, no. 5 (2017): 4056–61. http://dx.doi.org/10.1039/c6sc05399h.
Повний текст джерелаZgorzelak, Mikołaj, Jakub Grajewski, Jacek Gawroński, and 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, no. 16 (2019): 2301–4. http://dx.doi.org/10.1039/c8cc10184a.
Повний текст джерелаVerpaalen, Rob C. P., Michael G. Debije, Cees W. M. Bastiaansen, Haris Halilović, Tom A. P. Engels, and 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, no. 36 (2018): 17724–29. http://dx.doi.org/10.1039/c8ta06984k.
Повний текст джерелаHolland, Herbert L., Carl D. Turner, Peter R. Andreana, and Doan Nguyen. "Article." Canadian Journal of Chemistry 77, no. 4 (April 1, 1999): 463–71. http://dx.doi.org/10.1139/v99-068.
Повний текст джерелаMorrison, D. J., J. M. Blackwell, and W. E. Piers. "Mechanistic insights into perfluoroaryl borane-catalyzed allylstannations: Toward asymmetric induction with chiral boranes." Pure and Applied Chemistry 76, no. 3 (January 1, 2004): 615–23. http://dx.doi.org/10.1351/pac200476030615.
Повний текст джерелаMerelli, Bérangère, Laurence Menguy, Estelle Soubeyrand-Lenoir, and 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, no. 3 (2006): 95–107. http://dx.doi.org/10.1155/2006/698685.
Повний текст джерелаHan, Jung Tae, Jin Yong Lee та Jaesook Yun. "Asymmetric synthesis of γ-chiral borylalkanes via sequential reduction/hydroboration using a single copper catalyst". Chemical Science 11, № 33 (2020): 8961–65. http://dx.doi.org/10.1039/d0sc03759a.
Повний текст джерелаMimura, Shohei, Sho Mizushima, Yohei Shimizu та Masaya Sawamura. "Copper-catalyzed enantioselective conjugate reduction of α,β-unsaturated esters with chiral phenol–carbene ligands". Beilstein Journal of Organic Chemistry 16 (31 березня 2020): 537–43. http://dx.doi.org/10.3762/bjoc.16.50.
Повний текст джерелаSoundararajan, Karthikeyan, Helen Ratna Monica Jeyarajan, Raju Subimol Kamarajapurathu, and 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 (August 26, 2021): 2186–93. http://dx.doi.org/10.3762/bjoc.17.140.
Повний текст джерелаRamachary, Dhevalapally B., and Kodambahalli S. Shruthi. "Asymmetric synthesis of tetrahydroquinolines through supramolecular organocatalysis." Org. Biomol. Chem. 12, no. 25 (2014): 4300–4304. http://dx.doi.org/10.1039/c4ob00570h.
Повний текст джерелаUemura, Naohiro, Seiya Toyoda, Waku Shimizu, Yasushi Yoshida, Takashi Mino, and Masami Sakamoto. "Absolute Asymmetric Synthesis Involving Chiral Symmetry Breaking in Diels–Alder Reaction." Symmetry 12, no. 6 (June 1, 2020): 910. http://dx.doi.org/10.3390/sym12060910.
Повний текст джерелаBanerjee-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, no. 6395 (May 10, 2018): 1331–34. http://dx.doi.org/10.1126/science.aar4265.
Повний текст джерелаPuentes, Cira Mollings, and Thomas J. Wenzel. "Phosphated cyclodextrins as water-soluble chiral NMR solvating agents for cationic compounds." Beilstein Journal of Organic Chemistry 13 (January 6, 2017): 43–53. http://dx.doi.org/10.3762/bjoc.13.6.
Повний текст джерелаZhang, 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, no. 6460 (September 26, 2019): 1475–78. http://dx.doi.org/10.1126/science.aax5415.
Повний текст джерелаHong, Suk-Bong, and Frank M. Raushel. "Stereochemical preferences for chiral substrates by the bacterial phosphotriesterase." Chemico-Biological Interactions 119-120 (May 1999): 225–34. http://dx.doi.org/10.1016/s0009-2797(99)00031-9.
Повний текст джерелаYadav, J. S., and S. Nanda. "Novel chiral lipoxygenase substrates: design and synthesis. Part 2." Tetrahedron: Asymmetry 12, no. 23 (December 2001): 3223–34. http://dx.doi.org/10.1016/s0957-4166(02)00009-5.
Повний текст джерелаMurphy, James P., Mark Nieuwenhuyzen, Karen Reynolds, Pakala K. S. Sarma, and Paul J. Stevenson. "Chiral dienamides- substrates for asymmetric synthesis of amido cyclohexenes." Tetrahedron Letters 36, no. 52 (December 1995): 9533–36. http://dx.doi.org/10.1016/0040-4039(95)02040-3.
Повний текст джерелаMumtaz, Salma, Israel Cano, Nargis Mumtaz, Ahmed Abbas, Jairton Dupont, and Humaira Yasmeen Gondal. "Supramolecular interaction of non-racemic benzimidazolium based ion pairs with chiral substrates." Physical Chemistry Chemical Physics 20, no. 32 (2018): 20821–26. http://dx.doi.org/10.1039/c8cp03881c.
Повний текст джерелаZhou, Huan, Wenlei Zhao, Tao Zhang, Haodong Guo, Haizhou Huang, and Mingxin Chang. "Enantioselective Synthesis of 2-Substituted Pyrrolidines via Intramolecular Reductive Amination." Synthesis 51, no. 13 (May 7, 2019): 2713–19. http://dx.doi.org/10.1055/s-0037-1611533.
Повний текст джерелаMetallinos, Costa, Ngan Tran, and Dusty Cadwallader. "Diastereoselective Synthesis of Alkylated 1,4-Cyclohexadiene Esters Using Epimeric Pyrroloimidazolones." Synthesis 53, no. 01 (August 24, 2020): 182–92. http://dx.doi.org/10.1055/s-0040-1707351.
Повний текст джерелаZhang, Yue Cheng, Jing Yuan Gao, Nai Yue Shi, and 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 (November 2011): 1236–43. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.1236.
Повний текст джерелаThomas, Fabian, Dominik Steden, Alexander Eith, Alexander Hoffmann, and Sonja Herres-Pawlis. "Chiral bis(pyrazolyl)methane copper(I) complexes and their application in nitrene transfer reactions." Zeitschrift für Naturforschung B 76, no. 10-12 (October 29, 2021): 835–47. http://dx.doi.org/10.1515/znb-2021-0140.
Повний текст джерелаWu, Xianqing, Mohini Shrestha та Yifeng Chen. "Asymmetric Synthesis of α-Alkylated γ-Lactam via Nickel/8-Quinim-Catalyzed Reductive Alkyl-Carbamoylation of Unactivated Alkene". Synlett 32, № 10 (14 січня 2021): 955–61. http://dx.doi.org/10.1055/a-1353-7605.
Повний текст джерелаMakino, Yoshihide, Kousuke Inoue, Tohru Dairi, and Nobuya Itoh. "Engineering of Phenylacetaldehyde Reductase for Efficient Substrate Conversion in Concentrated 2-Propanol." Applied and Environmental Microbiology 71, no. 8 (August 2005): 4713–20. http://dx.doi.org/10.1128/aem.71.8.4713-4720.2005.
Повний текст джерела