Статті в журналах з теми "Olefin reactions"
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Liu, Qiang, Xufang Liu, and Bin Li. "Base-Metal-Catalyzed Olefin Isomerization Reactions." Synthesis 51, no. 06 (February 19, 2019): 1293–310. http://dx.doi.org/10.1055/s-0037-1612014.
Повний текст джерелаChow, Yuan L., and Xianen Cheng. "The dual pathway in photocycloaddition of 1,3-diketonatoboron difluorides: excimer reactions." Canadian Journal of Chemistry 69, no. 10 (October 1, 1991): 1575–83. http://dx.doi.org/10.1139/v91-232.
Повний текст джерелаVosloo, H. C. M., and J. A. K. Du Plessis. "A review of the mechanisms of the olefin metathesis reaction." Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie 7, no. 4 (March 17, 1988): 154–61. http://dx.doi.org/10.4102/satnt.v7i4.921.
Повний текст джерелаKřeček, Václav, Jiří Protiva, Miloš Buděšínský, Eva Klinotová, and Alois Vystrčil. "Preparation of C(18)-empiric 20,29,30-trinorlupane derivatives. 1H, 13C NMR and mass spectra." Collection of Czechoslovak Chemical Communications 51, no. 3 (1986): 621–35. http://dx.doi.org/10.1135/cccc19860621.
Повний текст джерелаSilva, Thiago S., and Fernando Coelho. "Methodologies for the synthesis of quaternary carbon centers via hydroalkylation of unactivated olefins: twenty years of advances." Beilstein Journal of Organic Chemistry 17 (July 7, 2021): 1565–90. http://dx.doi.org/10.3762/bjoc.17.112.
Повний текст джерелаPlessow, Philipp N., and Felix Studt. "Olefin methylation and cracking reactions in H-SSZ-13 investigated with ab initio and DFT calculations." Catalysis Science & Technology 8, no. 17 (2018): 4420–29. http://dx.doi.org/10.1039/c8cy01194j.
Повний текст джерелаGroso, Emilia, and Corinna Schindler. "Recent Advances in the Application of Ring-Closing Metathesis for the Synthesis of Unsaturated Nitrogen Heterocycles." Synthesis 51, no. 05 (February 8, 2019): 1100–1114. http://dx.doi.org/10.1055/s-0037-1611651.
Повний текст джерелаCory, Robert M., Paul C. Anderson, Murray D. Bailey, Fred R. McLaren, Richard M. Renneboog, and Brian R. Yamamoto. "Nitro-olefin bicycloannulation: one-step synthesis of tricyclo[3.2.1.02,7]octan-6-ones from cyclohexenones and of tricyclo[2.2.1.02,6]heptan-3-ones from cyclopentenones." Canadian Journal of Chemistry 63, no. 10 (October 1, 1985): 2618–27. http://dx.doi.org/10.1139/v85-435.
Повний текст джерелаRiehl, Paul S., Daniel J. Nasrallah, and Corinna S. Schindler. "Catalytic, transannular carbonyl-olefin metathesis reactions." Chemical Science 10, no. 44 (2019): 10267–74. http://dx.doi.org/10.1039/c9sc03716k.
Повний текст джерелаRemete, Attila Márió, Tamás T. Novák, Melinda Nonn, Matti Haukka, Ferenc Fülöp, and Loránd Kiss. "Synthesis of novel fluorinated building blocks via halofluorination and related reactions." Beilstein Journal of Organic Chemistry 16 (October 16, 2020): 2562–75. http://dx.doi.org/10.3762/bjoc.16.208.
Повний текст джерелаIuliis, Marco Zimmer De, Iain DG Watson, Andrei K. Yudin, and Robert H. Morris. "A DFT investigation into the origin of regioselectivity in palladium-catalyzed allylic amination." Canadian Journal of Chemistry 87, no. 1 (January 1, 2009): 54–62. http://dx.doi.org/10.1139/v08-078.
Повний текст джерелаYahyazadeh, Arash, Ajay K. Dalai, Wenping Ma, and Lifeng Zhang. "Fischer–Tropsch Synthesis for Light Olefins from Syngas: A Review of Catalyst Development." Reactions 2, no. 3 (July 21, 2021): 227–57. http://dx.doi.org/10.3390/reactions2030015.
Повний текст джерелаReany, Ofer, and N. Gabriel Lemcoff. "Light guided chemoselective olefin metathesis reactions." Pure and Applied Chemistry 89, no. 6 (June 27, 2017): 829–40. http://dx.doi.org/10.1515/pac-2016-1221.
Повний текст джерелаKlinot, Jiří, Jiří Liška, Alena Forgáčová, Miloš Buděšínský, Jiří Protiva, Stanislav Hilgard та Alois Vystrčil. "Acid-catalyzed rearrangements of an A(1)-nor-triterpenoid 2α,3α-epoxide". Collection of Czechoslovak Chemical Communications 54, № 2 (1989): 413–29. http://dx.doi.org/10.1135/cccc19890413.
Повний текст джерелаLemcoff, N., and Or Eivgi. "Turning the Light On: Recent Developments in Photoinduced Olefin Metathesis." Synthesis 50, no. 01 (September 21, 2017): 49–63. http://dx.doi.org/10.1055/s-0036-1589113.
Повний текст джерелаZhang, Xiaoqiao, Jianhong Gong, Xiaoli Wei, and Lingtao Liu. "Increased Light Olefin Production by Sequential Dehydrogenation and Cracking Reactions." Catalysts 12, no. 11 (November 17, 2022): 1457. http://dx.doi.org/10.3390/catal12111457.
Повний текст джерелаMatsuo, Takashi. "Functionalization of Ruthenium Olefin-Metathesis Catalysts for Interdisciplinary Studies in Chemistry and Biology." Catalysts 11, no. 3 (March 10, 2021): 359. http://dx.doi.org/10.3390/catal11030359.
Повний текст джерелаOss, Giulia, and Thanh Vinh Nguyen. "Iodonium-Catalyzed Carbonyl–Olefin Metathesis Reactions." Synlett 30, no. 17 (October 2019): 1966–70. http://dx.doi.org/10.1055/s-0039-1690297.
Повний текст джерелаTran, Uyen P. N., Giulia Oss, Domenic P. Pace, Junming Ho, and Thanh V. Nguyen. "Tropylium-promoted carbonyl–olefin metathesis reactions." Chemical Science 9, no. 23 (2018): 5145–51. http://dx.doi.org/10.1039/c8sc00907d.
Повний текст джерелаAbera Tsedalu, Atitegeb. "A Review on Olefin Metathesis Reactions as a Green Method for the Synthesis of Organic Compounds." Journal of Chemistry 2021 (September 4, 2021): 1–14. http://dx.doi.org/10.1155/2021/3590613.
Повний текст джерелаLiu, Wenqi, Sifan Cheng, Haripal Singh Malhi, Xinhua Gao, Zhenzhou Zhang, and Weifeng Tu. "Hydrogenation of CO2 to Olefins over Iron-Based Catalysts: A Review." Catalysts 12, no. 11 (November 14, 2022): 1432. http://dx.doi.org/10.3390/catal12111432.
Повний текст джерелаShin, Seunghoon. "The effect of acceptor-substituted alkynes in gold-catalyzed intermolecular reactions." Pure and Applied Chemistry 86, no. 3 (March 20, 2014): 373–79. http://dx.doi.org/10.1515/pac-2014-5039.
Повний текст джерелаFukusumi, Takanori, Natsuki Takei, Yubi Tateno, Takuya Aoki, Ai Ando, Kouhei Kozakai, Hiroko Shima, et al. "Ene-thiol reaction of C3-vinylated chlorophyll derivatives in the presence of oxygen: synthesis of C3-formyl-chlorins under mild conditions." Journal of Porphyrins and Phthalocyanines 17, no. 12 (December 2013): 1188–95. http://dx.doi.org/10.1142/s1088424613500983.
Повний текст джерелаDugkhuntod, Pannida, and Chularat Wattanakit. "A Comprehensive Review of the Applications of Hierarchical Zeolite Nanosheets and Nanoparticle Assemblies in Light Olefin Production." Catalysts 10, no. 2 (February 18, 2020): 245. http://dx.doi.org/10.3390/catal10020245.
Повний текст джерелаOpoku, Ernest, Richard Tia, and Evans Adei. "[3 + 2] versus [2 + 2] Addition: A Density Functional Theory Study on the Mechanistic Aspects of Transition Metal-Assisted Formation of 1,2-Dinitrosoalkanes." Journal of Chemistry 2016 (2016): 1–10. http://dx.doi.org/10.1155/2016/4538696.
Повний текст джерелаLi, Yuqi, Upal Kusari, Patrick J. Carroll, Mark G. Bradley, and Larry G. Sneddon. "Polyborane reactions in ionic liquids." Pure and Applied Chemistry 78, no. 7 (January 1, 2006): 1349–55. http://dx.doi.org/10.1351/pac200678071349.
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 джерелаDas, Aniruddha, Soumen Sarkar, Baitan Chakraborty, Abhishek Kar, and Umasish Jana. "Catalytic Alkyne/Alkene-Carbonyl Metathesis: Towards the Development of Green Organic Synthesis." Current Green Chemistry 7, no. 1 (May 15, 2020): 5–39. http://dx.doi.org/10.2174/2213346106666191105144019.
Повний текст джерелаSchindler, Corinna, and Jacob Ludwig. "Lewis Acid Catalyzed Carbonyl–Olefin Metathesis." Synlett 28, no. 13 (May 16, 2017): 1501–9. http://dx.doi.org/10.1055/s-0036-1588827.
Повний текст джерелаGordon, Christopher P., and Christophe Copéret. "Probing the Electronic Structure of Spectator Oxo Ligands by 17O NMR Spectroscopy." CHIMIA International Journal for Chemistry 74, no. 4 (April 29, 2020): 225–31. http://dx.doi.org/10.2533/chimia.2020.225.
Повний текст джерелаLiggio, J., and S. M. Li. "Reversible and irreversible processing of biogenic olefins on acidic aerosols." Atmospheric Chemistry and Physics Discussions 7, no. 4 (August 14, 2007): 11973–2009. http://dx.doi.org/10.5194/acpd-7-11973-2007.
Повний текст джерелаLiggio, J., and S. M. Li. "Reversible and irreversible processing of biogenic olefins on acidic aerosols." Atmospheric Chemistry and Physics 8, no. 7 (April 9, 2008): 2039–55. http://dx.doi.org/10.5194/acp-8-2039-2008.
Повний текст джерелаAstruc, Didier, Abdou K. Diallo, Sylvain Gatard, Liyuan Liang, Cátia Ornelas, Victor Martinez, Denise Méry, and Jaime Ruiz. "Olefin metathesis in nano-sized systems." Beilstein Journal of Organic Chemistry 7 (January 19, 2011): 94–103. http://dx.doi.org/10.3762/bjoc.7.13.
Повний текст джерелаLeigh, William J., Debbie T. Frendo, and Paul J. Klawunn. "Organic reactions in liquid crystalline solvents. 1. The thermal cis–trans isomerization of a bulky olefin in cholesteric liquid crystalline solvents." Canadian Journal of Chemistry 63, no. 8 (August 1, 1985): 2131–38. http://dx.doi.org/10.1139/v85-351.
Повний текст джерелаReymond, Sébastien, Laurent Ferrié, Amandine Guérinot, Patrice Capdevielle, and Janine Cossy. "Chemoselective reactions: Toward the synthesis of biologically active natural products with anticancer activities." Pure and Applied Chemistry 80, no. 8 (January 1, 2008): 1683–91. http://dx.doi.org/10.1351/pac200880081683.
Повний текст джерелаGrau, Benedikt W., and Svetlana B. Tsogoeva. "Iron-Catalyzed Carbonyl–Alkyne and Carbonyl–Olefin Metathesis Reactions." Catalysts 10, no. 9 (September 21, 2020): 1092. http://dx.doi.org/10.3390/catal10091092.
Повний текст джерелаAstruc, D. "The Olefin Metathesis Reactions in Dendrimers." Oil & Gas Science and Technology - Revue de l'IFP 62, no. 6 (October 30, 2007): 787–97. http://dx.doi.org/10.2516/ogst:2007055.
Повний текст джерелаZieliński, Grzegorz K., and Karol Grela. "Tandem Catalysis Utilizing Olefin Metathesis Reactions." Chemistry - A European Journal 22, no. 28 (June 14, 2016): 9417. http://dx.doi.org/10.1002/chem.201602627.
Повний текст джерелаZieliński, Grzegorz K., and Karol Grela. "Tandem Catalysis Utilizing Olefin Metathesis Reactions." Chemistry - A European Journal 22, no. 28 (May 20, 2016): 9440–54. http://dx.doi.org/10.1002/chem.201505136.
Повний текст джерелаBhat, Bilal A., and Bashir A. Shairgojray. "Applications of Micelles in Catalyzing Organic Reactions." Mini-Reviews in Organic Chemistry 17, no. 3 (April 28, 2020): 289–96. http://dx.doi.org/10.2174/1570193x16666181228112834.
Повний текст джерелаKakiuchi, Fumitoshi, Naoki Kimura, Shiori Katta, Yoichi Kitazawa, and Takuya Kochi. "Deuterium-Labeling Studies on the C–H/Olefin Coupling of Aromatic Ketones Catalyzed by Fe(PMe3)4." Synthesis 53, no. 18 (May 19, 2021): 3383–89. http://dx.doi.org/10.1055/s-0040-1706040.
Повний текст джерелаSales, Rita N., Samantha K. Callear, Pedro D. Vaz, and Carla D. Nunes. "Substrate–Solvent Crosstalk—Effects on Reaction Kinetics and Product Selectivity in Olefin Oxidation Catalysis." Chemistry 3, no. 3 (July 19, 2021): 753–64. http://dx.doi.org/10.3390/chemistry3030054.
Повний текст джерелаTanizume, Shusei, Toshihiro Yoshimura, Katsunori Ishii, and Mikihiro Nomura. "Control of Sequential MTO Reactions through an MFI-Type Zeolite Membrane Contactor." Membranes 10, no. 2 (February 7, 2020): 26. http://dx.doi.org/10.3390/membranes10020026.
Повний текст джерелаXia, Wei, Qi Sun, Shang Wen Liu, Lin Ping Qiang, and Yuan Cun Cui. "SAPO-34/SiO2 Catalysts for the Transformation of Ethanol into Propylene." Advanced Materials Research 1004-1005 (August 2014): 707–10. http://dx.doi.org/10.4028/www.scientific.net/amr.1004-1005.707.
Повний текст джерелаNicks, François, Yannick Borguet, Sébastien Delfosse, Dario Bicchielli, Lionel Delaude, Xavier Sauvage, and Albert Demonceau. "Microwave-Assisted Ruthenium-Catalyzed Reactions." Australian Journal of Chemistry 62, no. 3 (2009): 184. http://dx.doi.org/10.1071/ch08510.
Повний текст джерелаSabatino, Valerio, and Thomas R. Ward. "Aqueous olefin metathesis: recent developments and applications." Beilstein Journal of Organic Chemistry 15 (February 14, 2019): 445–68. http://dx.doi.org/10.3762/bjoc.15.39.
Повний текст джерелаNifant’ev, Ilya E., Ildar I. Salakhov та Pavel V. Ivchenko. "Transition Metal–(μ-Cl)–Aluminum Bonding in α-Olefin and Diene Chemistry". Molecules 27, № 21 (23 жовтня 2022): 7164. http://dx.doi.org/10.3390/molecules27217164.
Повний текст джерелаNifant’ev, Ilya E., Ildar I. Salakhov та Pavel V. Ivchenko. "Transition Metal–(μ-Cl)–Aluminum Bonding in α-Olefin and Diene Chemistry". Molecules 27, № 21 (23 жовтня 2022): 7164. http://dx.doi.org/10.3390/molecules27217164.
Повний текст джерелаNifant’ev, Ilya E., Ildar I. Salakhov та Pavel V. Ivchenko. "Transition Metal–(μ-Cl)–Aluminum Bonding in α-Olefin and Diene Chemistry". Molecules 27, № 21 (23 жовтня 2022): 7164. http://dx.doi.org/10.3390/molecules27217164.
Повний текст джерелаNifant’ev, Ilya E., Ildar I. Salakhov та Pavel V. Ivchenko. "Transition Metal–(μ-Cl)–Aluminum Bonding in α-Olefin and Diene Chemistry". Molecules 27, № 21 (23 жовтня 2022): 7164. http://dx.doi.org/10.3390/molecules27217164.
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