Статті в журналах з теми "Non-natural reactions"
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SAIGO, Kazuhiko, Atsushi SUDO, and Yukihiko HASHIMOTO. "Asymmetric Reactions Using Non-natural Chiral Auxiliaries." Journal of Synthetic Organic Chemistry, Japan 56, no. 5 (1998): 386–94. http://dx.doi.org/10.5059/yukigoseikyokaishi.56.386.
Повний текст джерелаHarms, Vanessa, Andreas Kirschning, and Jeroen S. Dickschat. "Nature-driven approaches to non-natural terpene analogues." Natural Product Reports 37, no. 8 (2020): 1080–97. http://dx.doi.org/10.1039/c9np00055k.
Повний текст джерелаHyster, Todd K. "Radical Biocatalysis: Using Non-Natural Single Electron Transfer Mechanisms to Access New Enzymatic Functions." Synlett 31, no. 03 (May 7, 2019): 248–54. http://dx.doi.org/10.1055/s-0037-1611818.
Повний текст джерелаHyster, Todd K., and Thomas R. Ward. "Genetic Optimization of Metalloenzymes: Enhancing Enzymes for Non-Natural Reactions." Angewandte Chemie International Edition 55, no. 26 (March 11, 2016): 7344–57. http://dx.doi.org/10.1002/anie.201508816.
Повний текст джерелаGober, Joshua G., and Eric M. Brustad. "Non-natural carbenoid and nitrenoid insertion reactions catalyzed by heme proteins." Current Opinion in Chemical Biology 35 (December 2016): 124–32. http://dx.doi.org/10.1016/j.cbpa.2016.09.004.
Повний текст джерелаWang, Zhipeng A., Yan-Yu Liang, and Ji-Shen Zheng. "Reductive Amination/Alkylation Reactions: The Recent Developments, Progresses, and Applications in Protein Chemical Biology Studies." Current Organic Synthesis 15, no. 6 (August 29, 2018): 755–61. http://dx.doi.org/10.2174/1570179415666180522093905.
Повний текст джерелаTaylor, James S., and Yung-Hian Leow. "Cutaneous Reactions to Rubber." Rubber Chemistry and Technology 73, no. 3 (July 1, 2000): 427–85. http://dx.doi.org/10.5254/1.3547600.
Повний текст джерелаXu, Guangcai, Michele Crotti, Thangavelu Saravanan, Kim M. Kataja, and Gerrit J. Poelarends. "Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase." Angewandte Chemie 132, no. 26 (April 14, 2020): 10460–64. http://dx.doi.org/10.1002/ange.202001373.
Повний текст джерелаXu, Guangcai, Michele Crotti, Thangavelu Saravanan, Kim M. Kataja, and Gerrit J. Poelarends. "Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase." Angewandte Chemie International Edition 59, no. 26 (April 14, 2020): 10374–78. http://dx.doi.org/10.1002/anie.202001373.
Повний текст джерелаFu, Peng, and John B. MacMillan. "Carpatizine, a novel bridged oxazine derivative generated by non-enzymatic reactions." Organic & Biomolecular Chemistry 15, no. 25 (2017): 5275–78. http://dx.doi.org/10.1039/c7ob01178d.
Повний текст джерелаBabbel, Justin, Courtney Ramos, Hannah Wangberg, Kate Luskin, and Ronald Simon. "Adverse reactions to food additives." Journal of Food Allergy 3, no. 1 (April 1, 2021): 8–23. http://dx.doi.org/10.2500/jfa.2021.3.210004.
Повний текст джерелаPerry, Christopher, Emmanuel L. C. de los Santos, Lona M. Alkhalaf, and Gregory L. Challis. "Rieske non-heme iron-dependent oxygenases catalyse diverse reactions in natural product biosynthesis." Natural Product Reports 35, no. 7 (2018): 622–32. http://dx.doi.org/10.1039/c8np00004b.
Повний текст джерелаRenata, Hans, Z. Jane Wang, and Frances H. Arnold. "Expanding the Enzyme Universe: Accessing Non-Natural Reactions by Mechanism-Guided Directed Evolution." Angewandte Chemie International Edition 54, no. 11 (February 3, 2015): 3351–67. http://dx.doi.org/10.1002/anie.201409470.
Повний текст джерелаKadokawa, Jun-ichi. "α-Glucan Phosphorylase-Catalyzed Enzymatic Reactions Using Analog Substrates to Synthesize Non-Natural Oligo- and Polysaccharides". Catalysts 8, № 10 (19 жовтня 2018): 473. http://dx.doi.org/10.3390/catal8100473.
Повний текст джерелаNakamura, Hitomi, Yudai Matsuda, and Ikuro Abe. "Unique chemistry of non-heme iron enzymes in fungal biosynthetic pathways." Natural Product Reports 35, no. 7 (2018): 633–45. http://dx.doi.org/10.1039/c7np00055c.
Повний текст джерелаWright, Dennis L. "Application of Olefin Metathesis to Organic Synthesis." Current Organic Chemistry 3, no. 3 (May 1999): 211–40. http://dx.doi.org/10.2174/1385272803666220202192919.
Повний текст джерелаFlom, Julie D., and Scott H. Sicherer. "Epidemiology of Cow’s Milk Allergy." Nutrients 11, no. 5 (May 10, 2019): 1051. http://dx.doi.org/10.3390/nu11051051.
Повний текст джерелаYu, Hui, та Feng Xu. "Non-noble metal-catalyzed cross-dehydrogenation coupling (CDC) involving ether α-C(sp3)–H to construct C–C bonds". Beilstein Journal of Organic Chemistry 19 (6 вересня 2023): 1259–88. http://dx.doi.org/10.3762/bjoc.19.94.
Повний текст джерелаCordero-Vargas, Alejandro, and Jeferson B. Mateus-Ruiz. "Visible-Light-Mediated Photoredox Reactions in the Total Synthesis of Natural Products." Synthesis 52, no. 21 (August 18, 2020): 3111–28. http://dx.doi.org/10.1055/s-0040-1707225.
Повний текст джерелаLegrand, Baptiste, Julie Aguesseau-Kondrotas, Matthieu Simon, and Ludovic Maillard. "Catalytic Foldamers: When the Structure Guides the Function." Catalysts 10, no. 6 (June 22, 2020): 700. http://dx.doi.org/10.3390/catal10060700.
Повний текст джерелаMiao, Xiao-Yu, Yong-Ji Hu, Fu-Rao Liu, Yuan-Yuan Sun, Die Sun, An-Xin Wu, and Yan-Ping Zhu. "Synthesis of Diversified Pyrazolo[3,4-b]pyridine Frameworks from 5-Aminopyrazoles and Alkynyl Aldehydes via Switchable C≡C Bond Activation Approaches." Molecules 27, no. 19 (September 27, 2022): 6381. http://dx.doi.org/10.3390/molecules27196381.
Повний текст джерелаBoreham, Christopher J., Dianne S. Edwards, Krystian Czado, Nadege Rollet, Liuqi Wang, Simon van der Wielen, David Champion, Richard Blewett, Andrew Feitz, and Paul A. Henson. "Hydrogen in Australian natural gas: occurrences, sources and resources." APPEA Journal 61, no. 1 (2021): 163. http://dx.doi.org/10.1071/aj20044.
Повний текст джерелаMukherjee, Jhumpa, and Sriparna Ray. "Structurally Characterized Non-Heme Fe(IV)Oxo Complexes: A Brief Overview." Asian Journal of Chemistry 34, no. 11 (2022): 2771–85. http://dx.doi.org/10.14233/ajchem.2022.23863.
Повний текст джерелаHanson, Jeffrey, Dan Groff, Abi Carlos, Hans Usman, Kevin Fong, Abigail Yu, Stephanie Armstrong, et al. "An Integrated In Vivo/In Vitro Protein Production Platform for Site-Specific Antibody Drug Conjugates." Bioengineering 10, no. 3 (February 28, 2023): 304. http://dx.doi.org/10.3390/bioengineering10030304.
Повний текст джерелаKeinan, Ehud, and Subhash C. Sinha. "Oxidative polycyclizations with rhenium(VII) oxides." Pure and Applied Chemistry 74, no. 1 (January 1, 2002): 93–105. http://dx.doi.org/10.1351/pac200274010093.
Повний текст джерелаTolmacheva, Anna S., and Georgy A. Nevinsky. "Essential Protective Role of Catalytically Active Antibodies (Abzymes) with Redox Antioxidant Functions in Animals and Humans." International Journal of Molecular Sciences 23, no. 7 (March 31, 2022): 3898. http://dx.doi.org/10.3390/ijms23073898.
Повний текст джерелаKolb, Benedikt, Daniela Silva dos Santos, Sanja Krause, Anna Zens, and Sabine Laschat. "Sequential hydrozirconation/Pd-catalyzed cross coupling of acyl chlorides towards conjugated (2E,4E)-dienones." Beilstein Journal of Organic Chemistry 19 (February 17, 2023): 176–85. http://dx.doi.org/10.3762/bjoc.19.17.
Повний текст джерелаTietze, L. F., G. Kettschau, J. A. Gewert, and A. Schuffenhauer. "Hetero-Diels-Aider Reactions of 1-0xa-1,3-butadienes." Current Organic Chemistry 2, no. 1 (January 1998): 19–62. http://dx.doi.org/10.2174/1385272802666220126210654.
Повний текст джерелаChaudhary, Ankita, Divya Mathur, Ritu Gaba, Raaina Pasricha, and Khyati Sharma. "Greening up organic reactions with caffeine: applications, recent developments, and future directions." RSC Advances 14, no. 13 (2024): 8932–62. http://dx.doi.org/10.1039/d4ra00432a.
Повний текст джерелаBornscheuer, Uwe T. "The fourth wave of biocatalysis is approaching." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 376, no. 2110 (November 27, 2017): 20170063. http://dx.doi.org/10.1098/rsta.2017.0063.
Повний текст джерелаFreindorf, Marek, and Elfi Kraka. "URVA and Local Mode Analysis of an Iridium Pincer Complex Efficiently Catalyzing the Hydrogenation of Carbon Dioxide." Inorganics 10, no. 12 (December 1, 2022): 234. http://dx.doi.org/10.3390/inorganics10120234.
Повний текст джерелаLiu, Fenghua, Lingling He, Sheng Dong, Jinsong Xuan, Qiu Cui, and Yingang Feng. "Artificial Small Molecules as Cofactors and Biomacromolecular Building Blocks in Synthetic Biology: Design, Synthesis, Applications, and Challenges." Molecules 28, no. 15 (August 3, 2023): 5850. http://dx.doi.org/10.3390/molecules28155850.
Повний текст джерелаJi, Yuemeng, Zhang Shi, Wenjian Li, Jiaxin Wang, Qiuju Shi, Yixin Li, Lei Gao, et al. "Aqueous-phase chemistry of glyoxal with multifunctional reduced nitrogen compounds: a potential missing route for secondary brown carbon." Atmospheric Chemistry and Physics 24, no. 5 (March 11, 2024): 3079–91. http://dx.doi.org/10.5194/acp-24-3079-2024.
Повний текст джерелаMoeller, Kevin D., Enqi Feng, Ruby Krueger, Zachary Medcalf, Polina Barzova, and Sarah Wagner. "Electrochemistry and Organic Synthesis: New Adventures with Olefin Coupling Reactions and Electrode Surfaces." ECS Meeting Abstracts MA2023-02, no. 52 (December 22, 2023): 2518. http://dx.doi.org/10.1149/ma2023-02522518mtgabs.
Повний текст джерелаTommaso, Morena Di, Arianna Miglio, Paolo Emidio Crisi, Andrea Boari, Francesca Rocconi, Maria Teresa Antognoni, and Alessia Luciani. "Frequency of Blood Types A, B and AB in a Population of Non-Pedigree Domestic Cats from Central Italy." Animals 10, no. 10 (October 21, 2020): 1937. http://dx.doi.org/10.3390/ani10101937.
Повний текст джерелаArnold, Frances H. "The nature of chemical innovation: new enzymes by evolution." Quarterly Reviews of Biophysics 48, no. 4 (July 16, 2015): 404–10. http://dx.doi.org/10.1017/s003358351500013x.
Повний текст джерелаGanley, Jack G., and Emily R. Derbyshire. "Linking Genes to Molecules in Eukaryotic Sources: An Endeavor to Expand Our Biosynthetic Repertoire." Molecules 25, no. 3 (January 31, 2020): 625. http://dx.doi.org/10.3390/molecules25030625.
Повний текст джерелаChiba, Kazuhiro. "(Organic and Biological Electrochemistry Division Manuel M. Baizer Award, Digital Presentation) Electron-Transfer-Triggered Smart Reactions Boost a Better Anthropocene." ECS Meeting Abstracts MA2022-01, no. 42 (July 7, 2022): 1827. http://dx.doi.org/10.1149/ma2022-01421827mtgabs.
Повний текст джерелаHirbodvash, Zohreh, and Pierre Berini. "Surface Plasmon Electrochemistry: Tutorial and Review." Chemosensors 11, no. 3 (March 19, 2023): 196. http://dx.doi.org/10.3390/chemosensors11030196.
Повний текст джерелаShokrollahi, Fatemeh, Kok Keong Lau, and Behzad Partoon. "Experimental Evaluation of Chemical Reactions Involved in Ultrasonic-Assisted Absorption of Bulk CO2." Processes 11, no. 12 (November 22, 2023): 3266. http://dx.doi.org/10.3390/pr11123266.
Повний текст джерелаMajhi, Sasadhar. "The Art of Total Synthesis of Bioactive Natural Products via Microwaves." Current Organic Chemistry 25, no. 9 (May 25, 2021): 1047–69. http://dx.doi.org/10.2174/1385272825666210303112302.
Повний текст джерелаRochussen, Jeremy, Gordon McTaggart-Cowan, and Patrick Kirchen. "Parametric study of pilot-ignited direct-injection natural gas combustion in an optically accessible heavy-duty engine." International Journal of Engine Research 21, no. 3 (March 25, 2019): 497–513. http://dx.doi.org/10.1177/1468087419836877.
Повний текст джерелаShoker, Roaa M. H., Wasan Hamza Al-Shammery, and S. R. Al-Aidy. "A Review Article: Free Radical and Replacement Synthetic Antioxidant by Natural Antioxidant." Journal for Research in Applied Sciences and Biotechnology 2, no. 2 (May 11, 2023): 206–11. http://dx.doi.org/10.55544/jrasb.2.2.29.
Повний текст джерелаHimiyama, Tomoki, and Yasunori Okamoto. "Artificial Metalloenzymes: From Selective Chemical Transformations to Biochemical Applications." Molecules 25, no. 13 (June 30, 2020): 2989. http://dx.doi.org/10.3390/molecules25132989.
Повний текст джерелаBelchinskaya, Larisa, Lyudmila Novikova, Vladimir Khokhlov, and Jen Ly Tkhi. "Contribution of Ion-Exchange and Non-Ion-Exchange Reactions to Sorption of Ammonium Ions by Natural and Activated Aluminosilicate Sorbent." Journal of Applied Chemistry 2013 (December 25, 2013): 1–9. http://dx.doi.org/10.1155/2013/789410.
Повний текст джерелаPätsch, Sebastian, Jevy V. Correia, Benedict J. Elvers, Mareile Steuer, and Carola Schulzke. "Inspired by Nature—Functional Analogues of Molybdenum and Tungsten-Dependent Oxidoreductases." Molecules 27, no. 12 (June 8, 2022): 3695. http://dx.doi.org/10.3390/molecules27123695.
Повний текст джерелаDondoni, Alessandro. "Selected Research Topics of the Dondoni Group over the Last Two Decades (2000–2020)." Synlett 31, no. 14 (May 7, 2020): 1361–71. http://dx.doi.org/10.1055/s-0040-1707107.
Повний текст джерелаGiovannini, Mattia, Francesca Mori, Simona Barni, Giulia Liccioli, Lucrezia Sarti, and Elio Novembre. "Tailored Sublingual Immunotherapy in a Monosensitized Child with Natural Rubber Latex Allergy." Pharmacology 105, no. 11-12 (2020): 719–22. http://dx.doi.org/10.1159/000508140.
Повний текст джерелаDerbaix, Christian M. "The Impact of Affective Reactions on Attitudes toward the Advertisement and the Brand: A Step toward Ecological Validity." Journal of Marketing Research 32, no. 4 (November 1995): 470–79. http://dx.doi.org/10.1177/002224379503200409.
Повний текст джерелаLan, Ping, Dong Xue Li, A. Ming Chen, Li Hong Lan, Tao Xie, and An Ping Liao. "The Effect of Microwave on the Physical and Chemical Properties of Cassava Starch." Advanced Materials Research 396-398 (November 2011): 2083–87. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.2083.
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