Статті в журналах з теми "Synthetic Transformation"
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Barrese, Eugenio, Elena Belluso, and Francesco Abbona. "On the transformation of synthetic diopside into chrysotile." European Journal of Mineralogy 9, no. 1 (December 30, 1996): 83–88. http://dx.doi.org/10.1127/ejm/9/1/0083.
Повний текст джерелаPatrylak, Lyubov, Serhii Konovalov, Stepan Zubenko, and Anzhela Yakovenko. "Transformation of Hexoses on Natural and Synthetic Zeolites." Chemistry & Chemical Technology 17, no. 2 (June 1, 2023): 287–93. http://dx.doi.org/10.23939/chcht17.02.287.
Повний текст джерелаAl-Jawaheri, Yassir, and Marc Colin Kimber. "The Rearrangement of Alkylallenes to 1,3-Dienes." Reactions 3, no. 1 (January 5, 2022): 70–86. http://dx.doi.org/10.3390/reactions3010006.
Повний текст джерелаSilva, Vera L. M., and Artur M. S. Silva. "Palladium-Catalysed Synthesis and Transformation of Quinolones." Molecules 24, no. 2 (January 9, 2019): 228. http://dx.doi.org/10.3390/molecules24020228.
Повний текст джерелаThompson, Mitchell G., William M. Moore, Niklas F. C. Hummel, Allison N. Pearson, Collin R. Barnum, Henrik V. Scheller, and Patrick M. Shih. "Agrobacterium tumefaciens: A Bacterium Primed for Synthetic Biology." BioDesign Research 2020 (May 26, 2020): 1–16. http://dx.doi.org/10.34133/2020/8189219.
Повний текст джерелаKhan, Umar Saeed, Abdul Manan, Nasrullah Khan, Amir Mahmood, and Abdur Rahim. "Transformation mechanism of magnetite nanoparticles." Materials Science-Poland 33, no. 2 (June 1, 2015): 278–85. http://dx.doi.org/10.1515/msp-2015-0037.
Повний текст джерелаHorn, Sabine, Katja Dahms, and Mathias O. Senge. "Synthetic transformations of porphyrins – Advances 2004-2007." Journal of Porphyrins and Phthalocyanines 12, no. 10 (October 2008): 1053–77. http://dx.doi.org/10.1142/s108842460800042x.
Повний текст джерелаNguyen, Thanh V. "Convenient Access to Hydroquinone and Quinone Derivatives from Cyclobutenedione Units." Australian Journal of Chemistry 63, no. 8 (2010): 1309. http://dx.doi.org/10.1071/ch10189.
Повний текст джерелаMoerschell, R. P., S. Tsunasawa, and F. Sherman. "Transformation of yeast with synthetic oligonucleotides." Proceedings of the National Academy of Sciences 85, no. 2 (January 1, 1988): 524–28. http://dx.doi.org/10.1073/pnas.85.2.524.
Повний текст джерелаGuo, Fenghai, Jayla A. Young, Mina S. Perez, Holden A. Hankerson, and Alex M. Chavez. "Progress on the Cu-Catalyzed 1,4-Conjugate Addition to Thiochromones." Catalysts 13, no. 4 (April 8, 2023): 713. http://dx.doi.org/10.3390/catal13040713.
Повний текст джерелаLee, Youjin V., Lingyuan Meng, Eleanor Ostroff, and Bozhi Tian. "Restructuring of ultra-thin branches in multi-nucleated silicon nanowires." Pure and Applied Chemistry 92, no. 12 (December 16, 2020): 1921–28. http://dx.doi.org/10.1515/pac-2020-0602.
Повний текст джерелаSharma, Yogesh Brijwashi, Bhakti Umesh Hirlekar, Yogesh P. Bharitkar, and Abhijit Hazra. "Lemon Juice: A Versatile Reusable Biocatalyst for the Synthesis of Bioactive Organic Compounds as well as Numerous Nanoparticles Based Catalytic System." Current Organic Chemistry 25, no. 10 (June 1, 2021): 1194–223. http://dx.doi.org/10.2174/1385272825666210317151732.
Повний текст джерелаPuglisi, A., E. Murtezi, G. Yilmaz, and Y. Yagci. "Synthesis of block copolymers by mechanistic transformation from photoinitiated cationic polymerization to a RAFT process." Polymer Chemistry 8, no. 47 (2017): 7307–10. http://dx.doi.org/10.1039/c7py01707c.
Повний текст джерелаCarlton, Robert A., Edward Orton, Charles E. Lyman, and James E. Roberts. "Qualitative Analysis of Solid Phase Synthesis Reaction Products by X-ray Spectrometry." Microscopy and Microanalysis 3, no. 6 (November 1997): 520–29. http://dx.doi.org/10.1017/s1431927697970409.
Повний текст джерелаWu, Jinghua, and Zhiqiang Ma. "Metal-hydride hydrogen atom transfer (MHAT) reactions in natural product synthesis." Organic Chemistry Frontiers 8, no. 24 (2021): 7050–76. http://dx.doi.org/10.1039/d1qo01139a.
Повний текст джерелаCai, Xiao-hua, Hongyan Zhang, and Hui Guo. "Denitrative Coupling Reaction: A Powerful Synthetic Tool in Functional Transformation." Current Organic Chemistry 23, no. 10 (August 16, 2019): 1131–50. http://dx.doi.org/10.2174/1385272823666190627114857.
Повний текст джерелаTakacs, J. M., S. C. Boito, and Y. C. Myoung. "Recent Applications of Catalytic Metal-Mediated Carbocyclizations in Asymmetric Synthesis." Current Organic Chemistry 2, no. 3 (May 1998): 233–54. http://dx.doi.org/10.2174/1385272802666220128192732.
Повний текст джерелаHsu, Ming-Tsung, Yi-Hung Liu, and Shiuh-Tzung Liu. "Synthesis of 2-Benzylidene-3-Pyrrolines and Their Synthetic Transformation." Reactions 1, no. 2 (October 16, 2020): 47–53. http://dx.doi.org/10.3390/reactions1020005.
Повний текст джерелаT. Mohd Ali, M., and . "Synthesis of -Hydroxy -Proline: Potential for Organocataly-sis Reactions." International Journal of Engineering & Technology 7, no. 4.14 (December 24, 2019): 237. http://dx.doi.org/10.14419/ijet.v7i4.14.27571.
Повний текст джерелаTaranenko, A. M. "GENETIC TRANSFORMATION OF PLANTS CONTAINING THE SYNTHETIC cry1Ab GENE ENCODING RESISTANCE TO LEPIDOPTERAN PESTS." Biotechnologia Acta 12, no. 6 (December 2019): 56–64. http://dx.doi.org/10.15407/biotech12.06.056.
Повний текст джерелаLiu, Leping, Bo Xu, and Gerald B. Hammond. "Construction of cyclic enones via gold-catalyzed oxygen transfer reactions." Beilstein Journal of Organic Chemistry 7 (May 13, 2011): 606–14. http://dx.doi.org/10.3762/bjoc.7.71.
Повний текст джерелаXu, Zhengkui, James L. Shull, and Waltraud M. Kriven. "Hot-stage Transmission Electron Microscopy Study of Phase Transformations in Hexacelsian (BaAl2Si2O8)." Journal of Materials Research 17, no. 6 (June 2002): 1287–97. http://dx.doi.org/10.1557/jmr.2002.0193.
Повний текст джерелаMalvar, H. "Comment on "Bilinear transformation by synthetic division"." IEEE Transactions on Automatic Control 30, no. 4 (April 1985): 416. http://dx.doi.org/10.1109/tac.1985.1103965.
Повний текст джерелаHagiwara, Hisahiro, Masashi Tsukagoshi, Takashi Hoshi, Toshio Suzuki, Toshihiro Hashimoto, and Yoshinori Asakawa. "Expedient Synthetic Transformation of Ptychantins into Forskolin." Synlett 2008, no. 6 (April 2008): 929–31. http://dx.doi.org/10.1055/s-2008-1042930.
Повний текст джерелаFerino, Italo, Roberto Monaci, Vincenzo Solinas, Lucio Forni, Antonio Rivoldini, and Luigi Sanseverino. "Transformation of 1-Butene over Synthetic Zeolites." Collection of Czechoslovak Chemical Communications 57, no. 4 (1992): 869–81. http://dx.doi.org/10.1135/cccc19920869.
Повний текст джерелаCajthaml, Tomáš, Zdena Křesinová, Kateřina Svobodová, Karel Sigler та Tomáš Řezanka. "Microbial transformation of synthetic estrogen 17α-ethinylestradiol". Environmental Pollution 157, № 12 (грудень 2009): 3325–35. http://dx.doi.org/10.1016/j.envpol.2009.06.027.
Повний текст джерелаOkuyama, Kenji, Mieko Ikeda, Shingo Yokoyama, Yanami Ochiai, Yusuke Hamada, and Masatsugu Shimomura. "Heat-indueed Crystal Transformation of Synthetic Bilayer." Chemistry Letters 17, no. 6 (June 5, 1988): 1013–16. http://dx.doi.org/10.1246/cl.1988.1013.
Повний текст джерелаNgapa, Yulius Dala, Sri Sugiarti, and Zaenal Abidin. "Hydrothermal Transformation of Natural Zeolite from Ende-NTT and Its Application as Adsorbent of Cationic Dye." Indonesian Journal of Chemistry 16, no. 2 (March 13, 2018): 138. http://dx.doi.org/10.22146/ijc.21156.
Повний текст джерелаRamírez-López, Sandra C., Manuel Alejandro Rentería-Gómez, Cesar R. Solorio Alvarado, and Rocío Gámez-Montaño. "Synthesis of Peptidomimetics via IMCR/Post-Transformation Strategy." Chemistry Proceedings 3, no. 1 (November 14, 2020): 4. http://dx.doi.org/10.3390/ecsoc-24-08396.
Повний текст джерелаDziuba, M., I. Navrotskaya, R. Brovko, and V. Doluda. "Methanol / Dimethyl Ether Catalytic Transformation Over Zn-modified H-ZSN-5 Zeolite." Bulletin of Science and Practice 6, no. 5 (May 15, 2020): 21–28. http://dx.doi.org/10.33619/2414-2948/54/02.
Повний текст джерелаIlić, Dušica, Vesna Nikolić, Mihajlo Stanković, Ljubiša Nikolić, Ljiljana Stanojević, Ivana Mladenović-Ranisavljević, and Andrija Šmelcerović. "Transformation of Synthetic Allicin: The Influence of Ultrasound, Microwaves, Different Solvents and Temperatures, and the Products Isolation." Scientific World Journal 2012 (2012): 1–7. http://dx.doi.org/10.1100/2012/561823.
Повний текст джерелаNegmatova, Kamola, Abdusattor Daminov, Abdusalam Umarov, and Nodira Аbed. "Synthesis of diamonds in the C – Mn - Ni - (H) system and the diamond-shaped mechanism." E3S Web of Conferences 264 (2021): 05003. http://dx.doi.org/10.1051/e3sconf/202126405003.
Повний текст джерелаChen, Xiaolan, Jian Han, Yan Zhu, Chunchen Yuan, Jingyu Zhang, and Yingsheng Zhao. "Transformation of masked benzyl alcohols to o-aminobenzaldehydes through C–H activation: a facile approach to quinazolines." Chemical Communications 52, no. 67 (2016): 10241–44. http://dx.doi.org/10.1039/c6cc05560e.
Повний текст джерелаKang, Minkyu, Minjun Bae, Sumin Park, Hwichan Hong, Taehyun Yoo, Yonghwan Kim, Myeongseok Jang, Young-Seok Kim, and Yuanzhe Piao. "Facile and scaleable transformation of Cu nanoparticles into high aspect ratio Cu oxide nanowires in methanol." RSC Advances 12, no. 18 (2022): 11526–33. http://dx.doi.org/10.1039/d2ra00510g.
Повний текст джерелаPieczara, Gabriela, Maciej Manecki, Grzegorz Rzepa, Olaf Borkiewicz, and Adam Gaweł. "Thermal Stability and Decomposition Products of P-Doped Ferrihydrite." Materials 13, no. 18 (September 16, 2020): 4113. http://dx.doi.org/10.3390/ma13184113.
Повний текст джерелаMattalia, Jean-Marc R. "The reductive decyanation reaction: an overview and recent developments." Beilstein Journal of Organic Chemistry 13 (February 13, 2017): 267–84. http://dx.doi.org/10.3762/bjoc.13.30.
Повний текст джерелаKnapp, Josef, Alexander Paulus, Carlos Lopez, and Thomas F. Eibert. "Comparison of non-convex cost functionals for the consideration of phase differences in phaseless near-field far-field transformations of measured antenna fields." Advances in Radio Science 15 (September 21, 2017): 11–19. http://dx.doi.org/10.5194/ars-15-11-2017.
Повний текст джерелаDu, Ke-Si, and Jing-Mei Huang. "Electrochemical dehydrogenation of hydrazines to azo compounds." Green Chemistry 21, no. 7 (2019): 1680–85. http://dx.doi.org/10.1039/c9gc00515c.
Повний текст джерелаChernov, S. V., E. E. Shul’ts, M. M. Shakirov, and G. A. Tolstikov. "Synthetic transformations of higher terpenoids: XII. Transformation of lambertianic acid into 14,16-epoxyabietane diterpenoids." Russian Journal of Organic Chemistry 42, no. 1 (January 2006): 36–41. http://dx.doi.org/10.1134/s1070428006010064.
Повний текст джерелаSharma, Sumit Kumar, Swati Mamgain, Burhanuddin Attarwala, and Aswani Yella. "ZnX2 mediated post-synthetic transformation of zero dimensional Cs4PbBr6 nanocrystals for opto-electronic applications." Nanoscale Advances 1, no. 7 (2019): 2502–9. http://dx.doi.org/10.1039/c9na00244h.
Повний текст джерелаJones, Lyn H., Nicholas W. Summerhill, Nigel A. Swain, and James E. Mills. "Aromatic chloride to nitrile transformation: medicinal and synthetic chemistry." MedChemComm 1, no. 5 (2010): 309–18. http://dx.doi.org/10.1039/c0md00135j.
Повний текст джерелаDominguez-Huerta, Alejandra, Xi-Jie Dai, Feng Zhou, Pierre Querard, Zihang Qiu, Sosthene Ung, Wenbo Liu, Jianbin Li, and Chao-Jun Li. "Exploration of new reaction tools for late-stage functionalization of complex chemicals." Canadian Journal of Chemistry 97, no. 2 (February 2019): 67–85. http://dx.doi.org/10.1139/cjc-2018-0357.
Повний текст джерелаSukdolak, S., S. Solujic-Sukdolak, and Lj Krstic. "Microbiological transformation of a synthetic benzofurane type lactone." Journal of the Serbian Chemical Society 65, no. 2 (2000): 103–11. http://dx.doi.org/10.2298/jsc0002103s.
Повний текст джерелаChandra, U., G. Parthasarathy, and P. Sharma. "SYNTHETIC CUBANITE CuFe2S3: PRESSURE-INDUCED TRANSFORMATION TO ISOCUBANITE." Canadian Mineralogist 48, no. 5 (October 1, 2010): 1137–47. http://dx.doi.org/10.3749/canmin.48.5.1137.
Повний текст джерелаLee, Jintae, and Henrik Pedersen. "Stable Genetic Transformation ofEschscholziaCalifornicaExpressing Synthetic Green Fluorescent Proteins." Biotechnology Progress 17, no. 2 (2001): 247–51. http://dx.doi.org/10.1021/bp010003v.
Повний текст джерелаGhaemmaghami, Sina, Joel C. Watts, Hoang-Oanh Nguyen, Shigenari Hayashi, Stephen J. DeArmond, and Stanley B. Prusiner. "Conformational Transformation and Selection of Synthetic Prion Strains." Journal of Molecular Biology 413, no. 3 (October 2011): 527–42. http://dx.doi.org/10.1016/j.jmb.2011.07.021.
Повний текст джерелаKumpulainen, S., M. L. Räisänen, F. Von Der Kammer, and T. Hofmann. "Ageing of synthetic and natural schwertmannites at pH 2—8." Clay Minerals 43, no. 3 (September 2008): 437–48. http://dx.doi.org/10.1180/claymin.2008.043.3.08.
Повний текст джерелаMou, Chung-Yuan, and Hong-Ping Lin. "Control of morphology in synthesizing mesoporous silica." Pure and Applied Chemistry 72, no. 1-2 (January 1, 2000): 137–46. http://dx.doi.org/10.1351/pac200072010137.
Повний текст джерелаDaniels, Peter, Bernd Wunder, Kurt Sahl, and Werner Schreyer. "Changing lattice metrics of synthetic cordierites: The metastable hexagonal to orthorhombic transformation sequence during isothermal annealing." European Journal of Mineralogy 6, no. 3 (June 7, 1994): 323–36. http://dx.doi.org/10.1127/ejm/6/3/0323.
Повний текст джерелаKalhapure, Vijay, Dhananjay Magar, Nishant Kothalkar, Tushar Khaladkar, and Abhijit Roychowdhury. "Synthesis of Substituted imidazo [1, 5-a] pyrimidine-2-(1H)-one Core Structure." Current Organic Synthesis 17, no. 1 (February 24, 2020): 23–28. http://dx.doi.org/10.2174/1389200220666191122103445.
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