Статті в журналах з теми "Methodology of synthesis"
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Shea, Kalyn M., Laurent Jaquinod, and Kevin M. Smith. "Dihydroporphyrin Synthesis: New Methodology†." Journal of Organic Chemistry 63, no. 20 (October 1998): 7013–21. http://dx.doi.org/10.1021/jo980965p.
Повний текст джерелаChikhradze, Nikoloz, Merab Nadirashvili, Tamar Iashvili, Akaki Gigineishvili, and Giorgi Beinashvili. "The Improvement of Picric Acid Synthesis Methodology." IOP Conference Series: Earth and Environmental Science 906, no. 1 (November 1, 2021): 012132. http://dx.doi.org/10.1088/1755-1315/906/1/012132.
Повний текст джерелаPadwa, A. "Tandem methodology for heterocyclic synthesis." Pure and Applied Chemistry 76, no. 11 (January 1, 2004): 1933–52. http://dx.doi.org/10.1351/pac200476111933.
Повний текст джерелаPrasad, M. V. Siva, and Ravi Gottipati. "Improve Accuracy of Intrusion Detection System Using the Synthesis Computing Classifier Methodology." Journal of Advances in Computer Networks 2, no. 4 (2014): 261–68. http://dx.doi.org/10.7763/jacn.2014.v2.123.
Повний текст джерелаPetrovčič, Jan, Chad Nicholas Ungarean, and David Sarlah. "Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids." Acta Chimica Slovenica 68, no. 2 (June 15, 2021): 247–67. http://dx.doi.org/10.17344/acsi.2021.6921.
Повний текст джерелаLI, TingTing, HongWei MA, ZhiYong WEI, Fang GUO, KaiHua SHEN, Hui NIU, and Yang LI. "Synthesis methodology of dendrigraft functional polymer." Chinese Science Bulletin 61, no. 31 (April 5, 2016): 3304–14. http://dx.doi.org/10.1360/n972015-01152.
Повний текст джерелаMcGuigan, Christopher, and Bernadette Swords. "Synthesis of phospholipids by phosphoramidite methodology." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1990): 783. http://dx.doi.org/10.1039/p19900000783.
Повний текст джерелаRussi, Jumar Lus, Mrio Lcio da Silva Martins, Luciano Schuch, Jos Renes Pinheiro, and Hlio Lees Hey. "Synthesis Methodology for Multipole ZVT Converters." IEEE Transactions on Industrial Electronics 54, no. 3 (June 2007): 1783–95. http://dx.doi.org/10.1109/tie.2007.895144.
Повний текст джерелаSHEA, K. M., L. JAQUINOD, and K. M. SMITH. "ChemInform Abstract: Dihydroporphyrin Synthesis: New Methodology." ChemInform 30, no. 9 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199909128.
Повний текст джерелаBellas, Vasilios, and Matthias Rehahn. "Universal Methodology for Block Copolymer Synthesis." Macromolecular Rapid Communications 28, no. 13 (July 2, 2007): 1415–21. http://dx.doi.org/10.1002/marc.200700127.
Повний текст джерелаRichetto, Katia C. S., and Cosme Roberto Moreira Silva. "Synthesis of Silicon Nitride Using Taguchi Planning Methodology." Materials Science Forum 591-593 (August 2008): 760–65. http://dx.doi.org/10.4028/www.scientific.net/msf.591-593.760.
Повний текст джерелаUmezawa, Taiki, and Fuyuhiko Matsuda. "Recent progress toward synthesis of chlorosulfolipids: total synthesis and methodology." Tetrahedron Letters 55, no. 19 (May 2014): 3003–12. http://dx.doi.org/10.1016/j.tetlet.2014.03.082.
Повний текст джерелаJurczak, Janusz, and Tomasz Bauer. "Glyoxylic acid derivatives in asymmetric synthesis." Pure and Applied Chemistry 72, no. 9 (January 1, 2000): 1589–96. http://dx.doi.org/10.1351/pac200072091589.
Повний текст джерелаShin, Eungsoo, and D. A. Streit. "Harmonic Synthesis Design Methodology for Dynamic Spring Balancing." Journal of Dynamic Systems, Measurement, and Control 118, no. 4 (December 1, 1996): 733–40. http://dx.doi.org/10.1115/1.2802350.
Повний текст джерелаVázquez, Alvaro J., Cristian Rodríguez, and N. Sbarbati Nudelman. "Convenient Methodology for the Synthesis of Trialkylhydrazines." Synthetic Communications 39, no. 22 (October 21, 2009): 3958–72. http://dx.doi.org/10.1080/00397910902738120.
Повний текст джерелаHU, Shanying. "Reaction path synthesis methodology for waste minimization." Science in China Series B 47, no. 3 (2004): 206. http://dx.doi.org/10.1360/03yb0204.
Повний текст джерелаManabe, Shino, Akiharu Ueki, and Yukishige Ito. "Polymer-supported oligosaccharide synthesis using ultrafiltration methodology." Chemical Communications, no. 35 (2007): 3673. http://dx.doi.org/10.1039/b705324j.
Повний текст джерелаKlein, J. O., E. Belhaire, C. Chappert, R. Cowburn, D. Read, and D. Petit. "Synthesis methodology for magnetic domain wall logic." International Journal of Electronics 95, no. 3 (March 2008): 249–63. http://dx.doi.org/10.1080/00207210701827988.
Повний текст джерелаBraslau, Rebecca, Anna Tsimelzon, and Jennifer Gewandter. "Novel Methodology for the Synthesis ofN-Alkoxyamines." Organic Letters 6, no. 13 (June 2004): 2233–35. http://dx.doi.org/10.1021/ol049271v.
Повний текст джерелаIsobe, Minoru, and Akinari Hamajima. "Ciguatoxin: developing the methodology for total synthesis." Natural Product Reports 27, no. 8 (2010): 1204. http://dx.doi.org/10.1039/b919467n.
Повний текст джерелаKatritzky, Alan R., Bogumila Rachwal, Stanislaw Rachwal, and Khalil A. Abboud. "Convenient Synthesis of Julolidines Using Benzotriazole Methodology." Journal of Organic Chemistry 61, no. 9 (January 1996): 3117–26. http://dx.doi.org/10.1021/jo9519118.
Повний текст джерелаLeighton, J., J. Spletstoser, and M. Zacuto. "Methodology for the Synthesis of Polyketide Fragments." Synfacts 2009, no. 03 (February 19, 2009): 0301. http://dx.doi.org/10.1055/s-0028-1087752.
Повний текст джерелаChessa, Gavino, and Alberto Scrivanti. "Synthesis of dendritic polypyridines using divergent methodology." Journal of Heterocyclic Chemistry 34, no. 6 (November 1997): 1851–55. http://dx.doi.org/10.1002/jhet.5570340635.
Повний текст джерелаKatritzky, Alan R., Delphine Semenzin, Baozhen Yang, and David P. M. Pleynet. "A novel synthesis of quinolinium saltsviabenzotriazole methodology." Journal of Heterocyclic Chemistry 35, no. 2 (March 1998): 467–70. http://dx.doi.org/10.1002/jhet.5570350234.
Повний текст джерелаKatritzky, Alan R., Samia Agamy, Baozhen Yang, and Guofang Qiu. "Synthesis of tetracyclic and pentacyclic phenothiazinesviabenzotriazole methodology." Journal of Heterocyclic Chemistry 36, no. 2 (March 1999): 473–76. http://dx.doi.org/10.1002/jhet.5570360223.
Повний текст джерелаMahajan, Pankaj S., Jyoti P. Mahajan, and Santosh B. Mhaske. "Malonic Ester Amide Synthesis: An Efficient Methodology for Synthesis of Amides." Synthetic Communications 43, no. 18 (June 3, 2013): 2508–16. http://dx.doi.org/10.1080/00397911.2012.717671.
Повний текст джерелаKeck, Gary E., Eugene P. Boden, and Michael R. Wiley. "Total synthesis of (+)-colletodiol: new methodology for the synthesis of macrolactones." Journal of Organic Chemistry 54, no. 4 (February 1989): 896–906. http://dx.doi.org/10.1021/jo00265a033.
Повний текст джерелаBoyle, F. Thomas, Zbigniew S. Matusiak, Owen Hares, and Donald A. Whiting. "Synthesis of tricyclospirodienones via spiroannulation; methodology for synthesis of aromatase inhibitors." Journal of the Chemical Society, Chemical Communications, no. 6 (1990): 518. http://dx.doi.org/10.1039/c39900000518.
Повний текст джерелаAlgatti, Mauricio A., Emerson Ferreira de Lucena, Élson de Campos, Rogério Pinto Mota, and Jerusa Góes Aragão Santana. "New Methodology in Modeling Ceramics." Advances in Science and Technology 63 (October 2010): 158–63. http://dx.doi.org/10.4028/www.scientific.net/ast.63.158.
Повний текст джерелаMcGarva, J. R., and G. Mullineux. "A New Methodology for Rapid Synthesis of Function Generators." Proceedings of the Institution of Mechanical Engineers, Part C: Journal of Mechanical Engineering Science 206, no. 6 (November 1992): 391–98. http://dx.doi.org/10.1243/pime_proc_1992_206_146_02.
Повний текст джерелаUlakpa, Wisdom Chukwuemeke. "Optimization of Biodiesel Synthesis using Response Surface Methodology." International Journal for Research in Applied Science and Engineering Technology 9, no. 5 (May 31, 2021): 1332–39. http://dx.doi.org/10.22214/ijraset.2021.34532.
Повний текст джерелаJoshi, Uday, Muriel Pipelier, Sebastien Naud, and Didier Dubreuil. "Ring Contraction Methodology for the Synthesis of Pyrroles." Current Organic Chemistry 9, no. 3 (February 1, 2005): 261–88. http://dx.doi.org/10.2174/1385272053369132.
Повний текст джерелаCudic, Predrag, and Maciej Stawikowski. "Pseudopeptide Synthesis via Fmoc Solid-Phase Synthetic Methodology." Mini-Reviews in Organic Chemistry 4, no. 4 (November 1, 2007): 268–80. http://dx.doi.org/10.2174/157019307782411716.
Повний текст джерелаVanelle, Patrice, Pascal Rathelot, José Maldonado, and Michel P. Crozet. "Synthesis of Various Substituted Nitroisoquinolines by SRN1 Methodology." HETEROCYCLES 45, no. 8 (1997): 1519. http://dx.doi.org/10.3987/com-97-7829.
Повний текст джерелаLiu, Jianping, Lewis N. Mander, and Masaji Koshioka. "Methodology for the synthesis of 11,13-hydroxy gibberellins." Arkivoc 2004, no. 10 (June 11, 2004): 68–79. http://dx.doi.org/10.3998/ark.5550190.0005.a08.
Повний текст джерелаMukhitdinov, Akmal, Kamoliddin Ziyaev, Janserik Omarov, and Shokhsanam Ismoilova. "Methodology of constructing driving cycles by the synthesis." E3S Web of Conferences 264 (2021): 01033. http://dx.doi.org/10.1051/e3sconf/202126401033.
Повний текст джерелаMonagheddu, M., N. Bertolino, P. Giuliani, C. Zanotti, and U. Anselmi Tamburini. "Ignition phenomena in combustion synthesis: An experimental methodology." Journal of Applied Physics 92, no. 1 (July 2002): 594–99. http://dx.doi.org/10.1063/1.1486254.
Повний текст джерелаBanerjee, Debasish. "A methodology for synthesis of recursive functional programs." ACM Transactions on Programming Languages and Systems 9, no. 3 (July 1987): 441–62. http://dx.doi.org/10.1145/24039.24071.
Повний текст джерелаWilliams, David, and Liangfeng Fu. "Methodology for the Synthesis of Substituted 1,3-Oxazoles." Synlett 2010, no. 04 (February 8, 2010): 591–94. http://dx.doi.org/10.1055/s-0029-1219374.
Повний текст джерелаNakabayashi, Kazuhiro. "Direct arylation polycondensation as conjugated polymer synthesis methodology." Polymer Journal 50, no. 7 (April 9, 2018): 475–83. http://dx.doi.org/10.1038/s41428-018-0039-5.
Повний текст джерелаKirovski, D., and M. Potkonjak. "Local watermarks: Methodology and application to behavioral synthesis." IEEE Transactions on Computer-Aided Design of Integrated Circuits and Systems 22, no. 9 (September 2003): 1277–84. http://dx.doi.org/10.1109/tcad.2003.816208.
Повний текст джерелаChowdhary, A., and R. K. Gupta. "A methodology for synthesis of data path circuits." IEEE Design & Test of Computers 19, no. 6 (November 2002): 90–100. http://dx.doi.org/10.1109/mdt.2002.1047748.
Повний текст джерелаBALL, HAYDN L., and PAOLO MASCAGNI. "Chemical synthesis and purification of proteins: a methodology." International Journal of Peptide and Protein Research 48, no. 1 (January 12, 2009): 31–47. http://dx.doi.org/10.1111/j.1399-3011.1996.tb01104.x.
Повний текст джерелаAnderson, James C., and Hilmi Namli. "Ambient Temperature Unsymmetrical Biaryl Synthesis Using Suzuki Methodology." Synlett 1995, no. 07 (July 1995): 765–66. http://dx.doi.org/10.1055/s-1995-5064.
Повний текст джерелаItzhaky, Shachar, Sumit Gulwani, Neil Immerman, and Mooly Sagiv. "A simple inductive synthesis methodology and its applications." ACM SIGPLAN Notices 45, no. 10 (October 17, 2010): 36–46. http://dx.doi.org/10.1145/1932682.1869463.
Повний текст джерелаFu, Zaiming, Hanglin Liu, and Nan Ren. "Methodology for digital synthesis of ultra‐narrow pulses." Electronics Letters 54, no. 16 (August 2018): 969–70. http://dx.doi.org/10.1049/el.2018.1218.
Повний текст джерелаJackson, Stephen K., Avedis Karadeolian, Alex B. Driega, and Michael A. Kerr. "Stereodivergent Methodology for the Synthesis of Complex Pyrrolidines." Journal of the American Chemical Society 130, no. 12 (March 2008): 4196–201. http://dx.doi.org/10.1021/ja710289k.
Повний текст джерелаWilliams, Craig, and Rebecca Pouwer. "Method in the Madness - Methodology from Total Synthesis." Synlett 23, no. 10 (May 29, 2012): 1446–58. http://dx.doi.org/10.1055/s-0031-1290967.
Повний текст джерелаJob, Andreas, Carsten F. Janeck, Wolfgang Bettray, René Peters, and Dieter Enders. "The SAMP-/RAMP-hydrazone methodology in asymmetric synthesis." Tetrahedron 58, no. 12 (March 2002): 2253–329. http://dx.doi.org/10.1016/s0040-4020(02)00080-7.
Повний текст джерелаPartridge, Benjamin M., Stephen P. Thomas, and Varinder K. Aggarwal. "Enantioenriched synthesis of Escitalopram using lithiation–borylation methodology." Tetrahedron 67, no. 52 (December 2011): 10082–88. http://dx.doi.org/10.1016/j.tet.2011.09.142.
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