Статті в журналах з теми "Organic synthesis problems"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Organic synthesis problems".
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.
Wang, Yi, Han Ding, and Ge Ging Xu. "Computer Aided Organic Synthesis Based on Graph Grammars." Applied Mechanics and Materials 411-414 (September 2013): 227–30. http://dx.doi.org/10.4028/www.scientific.net/amm.411-414.227.
Повний текст джерелаAmsad, L. N., S. Liliasari, A. Kadarohman, and R. E. Sardjono. "Revealing students’ problems in learning synthesis organic." Journal of Physics: Conference Series 1521 (March 2020): 042063. http://dx.doi.org/10.1088/1742-6596/1521/4/042063.
Повний текст джерелаSchaller, Chris P., Kate J. Graham, and T. Nicholas Jones. "Synthesis Road Map Problems in Organic Chemistry." Journal of Chemical Education 91, no. 12 (October 16, 2014): 2142–45. http://dx.doi.org/10.1021/ed400886k.
Повний текст джерелаKurth, Laurie L., and Mark J. Kurth. "Synthesis–Spectroscopy Roadmap Problems: Discovering Organic Chemistry." Journal of Chemical Education 91, no. 12 (September 23, 2014): 2137–41. http://dx.doi.org/10.1021/ed500109a.
Повний текст джерелаNakahara, Yoshiaki. "Problems and Progress in Glycopeptide Synthesis." Trends in Glycoscience and Glycotechnology 15, no. 85 (2003): 257–73. http://dx.doi.org/10.4052/tigg.15.257.
Повний текст джерелаFlynn, Alison B. "How do students work through organic synthesis learning activities?" Chem. Educ. Res. Pract. 15, no. 4 (2014): 747–62. http://dx.doi.org/10.1039/c4rp00143e.
Повний текст джерелаArslanov, Kh A., T. V. Tertychnaya, and S. B. Chernov. "Problems and Methods of Dating Low-Activity Samples by Liquid Scintillation Counting." Radiocarbon 35, no. 3 (1993): 393–98. http://dx.doi.org/10.1017/s0033822200060409.
Повний текст джерелаAmii, Hideki, Aiichiro Nagaki, and Jun-ichi Yoshida. "Flow microreactor synthesis in organo-fluorine chemistry." Beilstein Journal of Organic Chemistry 9 (December 5, 2013): 2793–802. http://dx.doi.org/10.3762/bjoc.9.314.
Повний текст джерелаHippe, Z. S., G. Fic, and M. Mazur. "A preliminary appraisal of selected problems in computer-assisted organic synthesis." Recueil des Travaux Chimiques des Pays-Bas 111, no. 6 (1992): 255–61. http://dx.doi.org/10.1002/recl.19921110603.
Повний текст джерелаHeifets, Abraham, and Igor Jurisica. "Construction of New Medicines via Game Proof Search." Proceedings of the AAAI Conference on Artificial Intelligence 26, no. 1 (September 20, 2021): 1564–70. http://dx.doi.org/10.1609/aaai.v26i1.8331.
Повний текст джерелаDong, Yuxin, Yifan Ji, and Ziyan Lai. "Carbon Dioxide Capture in Metal-Organic Frameworks." Highlights in Science, Engineering and Technology 21 (December 4, 2022): 50–56. http://dx.doi.org/10.54097/hset.v21i.3137.
Повний текст джерелаKurniawan, Yehezkiel Steven, Krisfian Tata Aneka Priyangga, Philip Anggo Krisbiantoro, and Arif Cahyo Imawan. "Green Chemistry Influences in Organic Synthesis : a Review." Journal of Multidisciplinary Applied Natural Science 1, no. 1 (January 7, 2021): 1–12. http://dx.doi.org/10.47352/jmans.v1i1.2.
Повний текст джерелаMa, Yuan Hui, Cheng Chun Tang, and Lei Zhang. "Property and Research Process of Metal-Organic Frameworks." Advanced Materials Research 427 (January 2012): 119–22. http://dx.doi.org/10.4028/www.scientific.net/amr.427.119.
Повний текст джерелаLima, Rafael C., Christian W. Lopes, Jhonny Villarroel-Rocha, Lindiane Bieseki, Karim Sapag, and Sibele B. C. Pergher. "Organic-Free Synthesis of Finned Mordenite Zeolite." Nanomaterials 12, no. 15 (July 29, 2022): 2623. http://dx.doi.org/10.3390/nano12152623.
Повний текст джерелаDembitsky, V. M., G. A. Tolstikov та M. Srebnik. "Boranes in Organic Chemistry 2. β-Aminoalkyl- and β-sulfanylalkylboranes in organic synthesis". Eurasian Chemico-Technological Journal 4, № 3 (30 червня 2017): 153. http://dx.doi.org/10.18321/ectj528.
Повний текст джерелаSalame, Issa I., Pauline Casino, and Natasha Hodges. "Examining Challenges that Students Face in Learning Organic Chemistry Synthesis." International Journal of Chemistry Education Research 3, no. 3 (May 22, 2020): 1–9. http://dx.doi.org/10.20885/ijcer.vol4.iss1.art1.
Повний текст джерелаNikolova, Marina. "PROBLEMS AND OPPORTUNITIES FOR REALIZATION OF BULGARIAN ORGANIC PRODUCTION." Trakia Journal of Sciences 17, Suppl.1 (2019): 259–67. http://dx.doi.org/10.15547/tjs.2019.s.01.042.
Повний текст джерелаRoulland, Emmanuel. "Tiacumicin B: An Antibiotic of Prime Importance and a Natural Product with an Inspiring Complex Structure." Synthesis 50, no. 21 (September 6, 2018): 4189–200. http://dx.doi.org/10.1055/s-0037-1609933.
Повний текст джерелаPramanik, Amit, Manabendra Saha, and Sanjay Bhar. "“On-Water” Catalyst-Free Ecofriendly Synthesis of the Hantzsch Dihydropyridines." ISRN Organic Chemistry 2012 (August 12, 2012): 1–7. http://dx.doi.org/10.5402/2012/342738.
Повний текст джерелаHIPPE, Z. S., G. FIC, and M. MAZUR. "ChemInform Abstract: A Preliminary Appraisal of Selected Problems in Computer-Assisted Organic Synthesis." ChemInform 23, no. 44 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199244300.
Повний текст джерелаWong, Chi-Huey, Randall L. Halcomb, Yoshitaka Ichikawa, and Tetsuya Kajimoto. "Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition(Part 1)." Angewandte Chemie International Edition in English 34, no. 4 (March 7, 1995): 412–32. http://dx.doi.org/10.1002/anie.199504121.
Повний текст джерелаWong, Chi-Huey, Randall L. Halcomb, Yoshitaka Ichikawa, and Tetsuya Kajimoto. "Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition(Part 2)." Angewandte Chemie International Edition in English 34, no. 5 (March 20, 1995): 521–46. http://dx.doi.org/10.1002/anie.199505211.
Повний текст джерелаDembitsky, V. M., G. A. Tolstikov та M. Srebnik. "Boranes in Organic Chemistry 1. α-Carbonylalkyl- and β-Oxyalkylboranes in Organic Synthesis". Eurasian Chemico-Technological Journal 4, № 2 (30 червня 2017): 87. http://dx.doi.org/10.18321/ectj522.
Повний текст джерелаZhang, Mengzhao, Taohua Leng, Yongjia Shen, and Chengyun Wang. "Reaction-based fluorescent probe for the selective and sensitive detection of thiophenols with a large Stokes shift and its application in water samples." Analyst 143, no. 3 (2018): 756–60. http://dx.doi.org/10.1039/c7an01994g.
Повний текст джерелаAnelli, Pier Lucio, Fernando Montanari, and Silvio Quici. "Polymer-supported cryptands. Problems arising in the synthesis of highly loaded polymers." Journal of Organic Chemistry 51, no. 25 (December 1986): 4910–14. http://dx.doi.org/10.1021/jo00375a028.
Повний текст джерелаShaik, Irfansha, and Jaco Van de Pol. "Classical Planning as QBF without Grounding." Proceedings of the International Conference on Automated Planning and Scheduling 32 (June 13, 2022): 329–37. http://dx.doi.org/10.1609/icaps.v32i1.19817.
Повний текст джерелаMoore, Max N., Mark Andrade, Anthony N. Scozzari, and Achim H. Krotz. "Overcoming Backpressure Problems during Solid-Phase Synthesis of Oligonucleotides." Organic Process Research & Development 8, no. 2 (March 2004): 271–74. http://dx.doi.org/10.1021/op030213j.
Повний текст джерелаLiang, Zhenye, Chen Tian, Xiaoxi Li, Liwei Cheng, Shanglei Feng, Lifeng Yang, Yingguo Yang, and Lina Li. "Organic–Inorganic Lead Halide Perovskite Single Crystal: From Synthesis to Applications." Nanomaterials 12, no. 23 (November 28, 2022): 4235. http://dx.doi.org/10.3390/nano12234235.
Повний текст джерелаSebati, Wilhemina, and Suprakas Ray. "Advances in Nanostructured Metal-Encapsulated Porous Organic-Polymer Composites for Catalyzed Organic Chemical Synthesis." Catalysts 8, no. 11 (October 24, 2018): 492. http://dx.doi.org/10.3390/catal8110492.
Повний текст джерелаYeon, Seung Ho, Bong Woo Lee, Sun Il Kim, and Il Nam Jung. "Problems and solutions involved in direct synthesis of allylchlorosilanes." Organometallics 12, no. 12 (December 1993): 4887–91. http://dx.doi.org/10.1021/om00036a031.
Повний текст джерелаBlatt, Celso. "Professor Remolo Ciola, a Master and a Genius." Brazilian Journal of Analytical Chemistry 8, no. 10Years (June 2021): 16–21. http://dx.doi.org/10.30744/brjac.2179-3425.letter-cblatt.
Повний текст джерелаDandapani, Sivaraman, Mario Jeske, and Dennis P. Curran. "Synthesis of All 16 Stereoisomers of Pinesaw Fly Sex Pheromones − Tools and Tactics for Solving Problems in Fluorous Mixture Synthesis." Journal of Organic Chemistry 70, no. 23 (November 2005): 9447–62. http://dx.doi.org/10.1021/jo051526a.
Повний текст джерелаPechkovsky, V. V., and L. S. Eshchenko. "Porous Phosphates of Trivalent Metals: Problems of Their Synthesis and Application." Phosphorus, Sulfur, and Silicon and the Related Elements 51, no. 1-4 (September 1990): 430. http://dx.doi.org/10.1080/10426509008040954.
Повний текст джерелаMolinari, Raffaele, Cristina Lavorato, and Pietro Argurio. "Visible-Light Photocatalysts and Their Perspectives for Building Photocatalytic Membrane Reactors for Various Liquid Phase Chemical Conversions." Catalysts 10, no. 11 (November 17, 2020): 1334. http://dx.doi.org/10.3390/catal10111334.
Повний текст джерелаGao, Xiang, Jiao Liu, Xin Zuo, Xinyue Feng, and Ying Gao. "Recent Advances in Synthesis of Benzothiazole Compounds Related to Green Chemistry." Molecules 25, no. 7 (April 5, 2020): 1675. http://dx.doi.org/10.3390/molecules25071675.
Повний текст джерелаFutaki, Shiroh, Kiwada Tatsuto, Yasuhisa Shiraishi, and Yukio Sugiura. "Total synthesis of artificial zinc-finger proteins: Problems and perspectives." Biopolymers 76, no. 2 (2004): 98–109. http://dx.doi.org/10.1002/bip.10562.
Повний текст джерелаBakayoko, Moussa, Loissi Kalakodio, Adiara Kalagodio, Bodjui Olivier Abo, Jean Pierre Muhoza, and El Moctar Ismaila. "Synthesis and characterization of the removal of organic pollutants in effluents." Reviews on Environmental Health 33, no. 2 (June 27, 2018): 135–46. http://dx.doi.org/10.1515/reveh-2018-0004.
Повний текст джерелаMilenkovic, Alexandra, Mathieu Macaud, Emmanuelle Schulz, Tamás Koltai, David Loffreda, Michel Vrinat, and Marc Lemaire. "How could organic synthesis help the understanding of the problems of deep hydrodesulfurization of gasoils?" Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry 3, no. 6 (November 2000): 459–63. http://dx.doi.org/10.1016/s1387-1609(00)00128-6.
Повний текст джерелаCassells, John M., and Peter J. Halling. "Protease-Catalyzed peptide synthesis in low-water organic two-phase systems and problems affecting it." Biotechnology and Bioengineering 33, no. 11 (May 1989): 1489–94. http://dx.doi.org/10.1002/bit.260331117.
Повний текст джерелаWONG, C. H., R. L. HALCOMB, Y. ICHIKAWA, and T. KAJIMOTO. "ChemInform Abstract: Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition. Part 1." ChemInform 26, no. 27 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199527323.
Повний текст джерелаWONG, C. H., R. L. HALCOMB, Y. ICHIKAWA, and T. KAJIMOTO. "ChemInform Abstract: Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition. Part 2." ChemInform 26, no. 29 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199529335.
Повний текст джерелаSantos, Filipa, Luís C. Branco, and Ana Rita C. Duarte. "Organic Salts Based on Isoniazid Drug: Synthesis, Bioavailability and Cytotoxicity Studies." Pharmaceutics 12, no. 10 (October 10, 2020): 952. http://dx.doi.org/10.3390/pharmaceutics12100952.
Повний текст джерелаKostadinova, N. "THE BIOAGRICULTURE-ECOLOGY SYNERGY." Trakia Journal of Sciences 18, Suppl.1 (2020): 560–63. http://dx.doi.org/10.15547/tjs.2020.s.01.089.
Повний текст джерелаJones, David J., Eileen M. O’Leary, and Timothy P. O’Sullivan. "An improved synthesis of adefovir and related analogues." Beilstein Journal of Organic Chemistry 15 (March 29, 2019): 801–10. http://dx.doi.org/10.3762/bjoc.15.77.
Повний текст джерелаAnderson, Shannon Y. C., Whitney S. Y. Ong, and Jennifer L. Momsen. "Support for instructional scaffolding with 1H NMR spectral features in organic chemistry textbook problems." Chemistry Education Research and Practice 21, no. 3 (2020): 749–64. http://dx.doi.org/10.1039/c9rp00252a.
Повний текст джерелаDyudeeva, E. S., A. S. Pavlova, M. S. Kupryushkin, D. V. Pyshnyi, and I. A. Pyshnaya. "Problems of the Synthesis of Oligonucleotide Derivatives in the Realization of the Anchimeric Effect." Russian Journal of Bioorganic Chemistry 47, no. 2 (March 2021): 505–13. http://dx.doi.org/10.1134/s1068162021020096.
Повний текст джерелаBagirov, Gyulyara, S. R. Rafiyeva, F. A. Nasirov, G. N. Hasanova, A. D. Kuliyev, A. M. Tagiyeva, and N. F. Janibayov. "DIRECT SYNTHESIS OF 1.4-CIS POLYBUTADIENE WITH APPLICATION OF HETEROGENIZED DITHIOSYSTEM." JOURNAL OF ADVANCES IN CHEMISTRY 11, no. 6 (September 16, 2015): 3678–84. http://dx.doi.org/10.24297/jac.v11i6.856.
Повний текст джерелаKardooni, Rezvan, and Ali Reza Kiasat. "Polyethylene Glycol as a Green and Biocompatible Reaction Media for the Catalyst Free Synthesis of Organic Compounds." Current Organic Chemistry 24, no. 12 (September 22, 2020): 1275–314. http://dx.doi.org/10.2174/1385272824999200605161840.
Повний текст джерелаRubab, Laila, Ayesha Anum, Sami A. Al-Hussain, Ali Irfan, Sajjad Ahmad, Sami Ullah, Aamal A. Al-Mutairi, and Magdi E. A. Zaki. "Green Chemistry in Organic Synthesis: Recent Update on Green Catalytic Approaches in Synthesis of 1,2,4-Thiadiazoles." Catalysts 12, no. 11 (October 29, 2022): 1329. http://dx.doi.org/10.3390/catal12111329.
Повний текст джерелаYuliyanto, Eko, Yosef Wijoyo, Enade Perdana Istyastono, and Fitria Fatichatul Hidayah. "REFLEKSI PRAKTIKUM KIMIA ORGANIK CALON PENDIDIK KIMIA MENGGUNAKAN REKAMAN VIDEO." JURNAL PENDIDIKAN SAINS (JPS) 6, no. 2 (November 16, 2018): 76. http://dx.doi.org/10.26714/jps.6.2.2018.76-83.
Повний текст джерела