Статті в журналах з теми "Carbocyclic systems"
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Boyd, Derek R., Narain D. Sharma, Ludmila V. Modyanova, Jonathan G. Carroll, John F. Malone, Christopher CR Allen, John TG Hamilton, David T. Gibson, Rebecca E. Parales, and Howard Dalton. "Dioxygenase-catalyzed cis-dihydroxylation of pyridine-ring systems." Canadian Journal of Chemistry 80, no. 6 (June 1, 2002): 589–600. http://dx.doi.org/10.1139/v02-062.
Повний текст джерелаWilliams, Andrew C. "The synthesis of carbocyclic aromatic systems." Contemporary Organic Synthesis 3, no. 6 (1996): 535. http://dx.doi.org/10.1039/co9960300535.
Повний текст джерелаAndo, Wataru. "Polyorganosilicon Compounds in Strained Carbocyclic Systems." Bulletin of the Chemical Society of Japan 69, no. 1 (January 1996): 1–16. http://dx.doi.org/10.1246/bcsj.69.1.
Повний текст джерелаGleiter, Rolf, та Daniel B. Werz. "Reactions of Metal-Complexed Carbocyclic 4π Systems". Organometallics 24, № 18 (серпень 2005): 4316–29. http://dx.doi.org/10.1021/om0504351.
Повний текст джерелаWILLIAMS, A. C. "ChemInform Abstract: The Synthesis of Carbocyclic Aromatic Systems." ChemInform 28, no. 19 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199719292.
Повний текст джерелаANDO, W. "ChemInform Abstract: Polyorganosilicon Compounds in Strained Carbocyclic Systems." ChemInform 27, no. 17 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199617312.
Повний текст джерелаAl Mamari, Hamad H. "Ir-Catalyzed ortho-C-H Borylation of Aromatic C(sp2)-H Bonds of Carbocyclic Compounds Assisted by N-Bearing Directing Groups." Reactions 5, no. 2 (May 1, 2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.
Повний текст джерелаErian, Ayman W., Yvette A. Issac, and Sherif M. Sherif. "A Novel Synthesis of Sulfone Systems as Antimicrobial Agents." Zeitschrift für Naturforschung B 55, no. 1 (January 1, 2000): 127–32. http://dx.doi.org/10.1515/znb-2000-0119.
Повний текст джерелаDoraghi, Fatemeh, Mohammad Mahdi Aghanour Ashtiani, Fatemeh Moradkhani, Bagher Larijani та Mohammad Mahdavi. "Developments and applications of α-bromonitrostyrenes in organic syntheses". RSC Advances 14, № 21 (2024): 14835–46. http://dx.doi.org/10.1039/d4ra02474e.
Повний текст джерелаWang, Zheng, Yanping Ma, Jingjing Guo, Qingbin Liu, Gregory A. Solan, Tongling Liang, and Wen-Hua Sun. "Bis(imino)pyridines fused with 6- and 7-membered carbocylic rings as N,N,N-scaffolds for cobalt ethylene polymerization catalysts." Dalton Transactions 48, no. 8 (2019): 2582–91. http://dx.doi.org/10.1039/c8dt04892d.
Повний текст джерелаTV, Ovaska. "Utilization of Tandem Oxyanionic Cyclization/Claisen Rearrangement Strategies for the Construction of Seven and Eight-Membered Carbocyclic Ring Systems." Medicinal and Analytical Chemistry International Journal 7, no. 1 (January 23, 2023): 1–6. http://dx.doi.org/10.23880/macij-16000178.
Повний текст джерелаRawal, Viresh H., Randall C. Newton, and Venkat Krishnamurthy. "Synthesis of carbocyclic systems via radical-induced epoxide fragmentation." Journal of Organic Chemistry 55, no. 18 (August 1990): 5181–83. http://dx.doi.org/10.1021/jo00305a001.
Повний текст джерелаGao, Fuye, and D. Jean Burnell. "Diverse carbocyclic systems using geminal acylation as a key process." Tetrahedron Letters 48, no. 46 (November 2007): 8185–88. http://dx.doi.org/10.1016/j.tetlet.2007.09.089.
Повний текст джерелаYavari, Issa, and Aliyeh Khajeh-Khezri. "Recent Advances in the Synthesis of Hetero- and Carbocyclic Compounds and Complexes Based on Acenaphthylene-1,2-dione." Synthesis 50, no. 20 (August 16, 2018): 3947–73. http://dx.doi.org/10.1055/s-0037-1610209.
Повний текст джерелаLautens, Mark, Dino Alberico, Cyril Bressy, Yuan-Qing Fang, Brian Mariampillai, and Thorsten Wilhelm. "Palladium-catalyzed ring-forming reactions: Methods and applications." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 351–61. http://dx.doi.org/10.1351/pac200678020351.
Повний текст джерелаSoares, Maria I. L., Ana L. Cardoso, and Teresa M. V. D. Pinho e Melo. "Diels–Alder Cycloaddition Reactions in Sustainable Media." Molecules 27, no. 4 (February 15, 2022): 1304. http://dx.doi.org/10.3390/molecules27041304.
Повний текст джерелаGahman, Timothy C., and Larry E. Overman. "Stereoselective synthesis of carbocyclic ring systems by pinacol-terminated Prins cyclizations." Tetrahedron 58, no. 32 (August 2002): 6473–83. http://dx.doi.org/10.1016/s0040-4020(02)00658-0.
Повний текст джерелаKlimova, Elena I., Marcos Martı́nez Garcı́a, Tatiana Klimova, Cecilio Alvarez Toledano, Ruben Alfredo Toscano, and Lena Ruı́z Ramı́rez. "Synthesis of ‘three-petal’ carbocyclic systems based on s-cis-diferrocenyltrienes." Journal of Organometallic Chemistry 649, no. 1 (April 2002): 86–93. http://dx.doi.org/10.1016/s0022-328x(02)01127-0.
Повний текст джерелаRAWAL, V. H., R. C. NEWTON, and V. KRISHNAMURTHY. "ChemInform Abstract: Synthesis of Carbocyclic Systems via Radical-Induced Epoxide Fragmentation." ChemInform 22, no. 6 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199106147.
Повний текст джерелаGriffith, Daniel R., and Aaron H. Shoemaker. "Synthetic Approaches to Non-Tropane, Bridged, Azapolycyclic Ring Systems Containing Seven-Membered Carbocycles." Synthesis 53, no. 01 (September 11, 2020): 65–78. http://dx.doi.org/10.1055/s-0040-1707385.
Повний текст джерелаWu, Xiang, Ming-Li Li, Dian-Feng Chen, and Shu-Sen Chen. "Enantioselective Construction of [6,5,6]-Carbocyclic Systems by Organo/Metal-Catalyzed Sequential Reactions." Journal of Organic Chemistry 79, no. 10 (April 25, 2014): 4743–50. http://dx.doi.org/10.1021/jo5006729.
Повний текст джерелаGarcia-Fandiño, Rebeca, Eva M. Codesido, Eduardo Sobarzo-Sánchez, Luis Castedo, and Juan R. Granja. "Tandem RCM of Dienynes for the Construction of Taxol-Type Carbocyclic Systems." Organic Letters 6, no. 2 (January 2004): 193–96. http://dx.doi.org/10.1021/ol036062m.
Повний текст джерелаWilletts, Andrew. "Bicyclo[3.2.0]carbocyclic Molecules and Redox Biotransformations: The Evolution of Closed-Loop Artificial Linear Biocatalytic Cascades and Related Redox-Neutral Systems." Molecules 28, no. 21 (October 24, 2023): 7249. http://dx.doi.org/10.3390/molecules28217249.
Повний текст джерелаDurakov, S. A., A. A. Kolobov, and V. R. Flid. "Features of heterogeneous catalytic transformations of strained carbocyclic compounds of the norbornene series." Fine Chemical Technologies 17, no. 4 (September 30, 2022): 275–97. http://dx.doi.org/10.32362/2410-6593-2022-17-4-275-297.
Повний текст джерелаChen, Jia-Rong, Xiao-Qiang Hu, Liang-Qiu Lu, and Wen-Jing Xiao. "Formal [4+1] Annulation Reactions in the Synthesis of Carbocyclic and Heterocyclic Systems." Chemical Reviews 115, no. 11 (May 20, 2015): 5301–65. http://dx.doi.org/10.1021/cr5006974.
Повний текст джерелаGahman, Timothy C., and Larry E. Overman. "ChemInform Abstract: Stereoselective Synthesis of Carbocyclic Ring Systems by Pinacol-Terminated Prins Cyclizations." ChemInform 33, no. 50 (May 18, 2010): no. http://dx.doi.org/10.1002/chin.200250061.
Повний текст джерелаKRYGOWSKI, T. M., та M. CYRANSKI. "ChemInform Abstract: Aromatic Character of Carbocyclic π-Electron Systems Deduced from Molecular Geometry". ChemInform 28, № 42 (3 серпня 2010): no. http://dx.doi.org/10.1002/chin.199742352.
Повний текст джерелаMalik, Arfa Abrar, Wenhong Yang, Zhifeng Ma, and Wen-Hua Sun. "The Catalytic Activities of Carbocyclic Fused Pyridineimine Nickel Complexes Analogues in Ethylene Polymerization by Modeling Study." Catalysts 9, no. 6 (June 12, 2019): 520. http://dx.doi.org/10.3390/catal9060520.
Повний текст джерелаSotomayor, N., and E. Lete. "Aryl and Heteroaryllithium Compounds by Metal - Halogen Exchange. Synthesis of Carbocyclic and Heterocyclic Systems." Current Organic Chemistry 7, no. 3 (February 1, 2003): 275–300. http://dx.doi.org/10.2174/1385272033372987.
Повний текст джерелаDanishefsky, Samuel J., and James E. Audia. "An application of the ireland reaction to the stereospecific synthesis of fused carbocyclic systems." Tetrahedron Letters 29, no. 12 (January 1988): 1371–74. http://dx.doi.org/10.1016/s0040-4039(00)80299-3.
Повний текст джерелаBarluenga, José, Ana Álvarez-Fernández, Tatiana Suárez-Rodríguez, Ángel L. Suárez-Sobrino, and Miguel Tomás. "A Simple Metal-Promoted Three-Step Access to n/5/m Angular Carbocyclic Systems." Organic Letters 15, no. 3 (January 11, 2013): 488–91. http://dx.doi.org/10.1021/ol303269r.
Повний текст джерелаXuan, Jun, Liang-Qiu Lu, Jia-Rong Chen, and Wen-Jing Xiao. "Visible-Light-Driven Photoredox Catalysis in the Construction of Carbocyclic and Heterocyclic Ring Systems." European Journal of Organic Chemistry 2013, no. 30 (July 9, 2013): 6755–70. http://dx.doi.org/10.1002/ejoc.201300596.
Повний текст джерелаWu, Xiang, Ming-Li Li, Dian-Feng Chen, and Shu-Sen Chen. "ChemInform Abstract: Enantioselective Construction of [6,5,6]-Carbocyclic Systems by Organo/Metal-Catalyzed Sequential Reactions." ChemInform 45, no. 43 (October 10, 2014): no. http://dx.doi.org/10.1002/chin.201443081.
Повний текст джерелаLash, Timothy D. "Organometallic Chemistry within the Structured Environment Provided by the Macrocyclic Cores of Carbaporphyrins and Related Systems." Molecules 28, no. 3 (February 3, 2023): 1496. http://dx.doi.org/10.3390/molecules28031496.
Повний текст джерелаBailey, William F., and Justin D. Fair. "Intramolecular carbolithiation cascades as a route to a highly strained carbocyclic framework: competition between 5-exo-trig ring closure and proton transfer." Beilstein Journal of Organic Chemistry 9 (March 14, 2013): 537–43. http://dx.doi.org/10.3762/bjoc.9.59.
Повний текст джерелаZander, M. "The Intra-annular Internal Heavy-atom Effect on the Fluorescence and Phosphorescence Properties of Oxygen, Sulphur or Selenium Containing Heterocyclic Systems Related to Dibenzo [b,n] perylene." Zeitschrift für Naturforschung A 44, no. 11 (November 1, 1989): 1116–18. http://dx.doi.org/10.1515/zna-1989-1113.
Повний текст джерелаChen, Jia-Rong, Xiao-Qiang Hu, Liang-Qiu Lu, and Wen-Jing Xiao. "ChemInform Abstract: Formal [4+1] Annulation Reactions in the Synthesis of Carbocyclic and Heterocyclic Systems." ChemInform 46, no. 35 (August 13, 2015): no. http://dx.doi.org/10.1002/chin.201535268.
Повний текст джерелаCieśla, J. M., R. Stolarski, and D. Shugar. "Cyclic phosphates of some antiviral acyclonucleosides: relationship between conformation and substrate/inhibitor properties in some enzyme systems." Acta Biochimica Polonica 40, no. 2 (June 30, 1993): 251–60. http://dx.doi.org/10.18388/abp.1993_4826.
Повний текст джерелаHarrowven, David, Wei Sun, and Dharyl Wilson. "Steric Buttressing Changes Torquospecificity in Thermal Cyclobutenone Rearrangements, Providing New Opportunities for 5H-Furanone Synthesis." Synthesis 49, no. 14 (June 13, 2017): 3091–106. http://dx.doi.org/10.1055/s-0036-1588850.
Повний текст джерелаChambournier, Gilles, Venkat Krishnamurthy, and Viresh H. Rawal. "Radical Induced Cyclopropane Fragmentation—H-Abstraction—Cyclization Cascade: Synthesis of Carbocyclic Systems Containing Bridgehead Methyl Groups." Tetrahedron Letters 38, no. 36 (September 1997): 6313–16. http://dx.doi.org/10.1016/s0040-4039(97)01450-0.
Повний текст джерелаXuan, Jun, Liang-Qiu Lu, Jia-Rong Chen, and Wen-Jing Xiao. "ChemInform Abstract: Visible-Light-Driven Photoredox Catalysis in the Construction of Carbocyclic and Heterocyclic Ring Systems." ChemInform 45, no. 1 (December 12, 2013): no. http://dx.doi.org/10.1002/chin.201401252.
Повний текст джерелаBarluenga, Jose, Ana Alvarez-Fernandez, Tatiana Suarez-Rodriguez, Angel L. Suarez-Sobrino, and Miguel Tomas. "ChemInform Abstract: A Simple Metal-Promoted Three-Step Access to n/5/m Angular Carbocyclic Systems." ChemInform 44, no. 24 (May 23, 2013): no. http://dx.doi.org/10.1002/chin.201324043.
Повний текст джерелаTrost, Barry M., Zhongxing Huang, and Ganesh M. Murhade. "Catalytic palladium-oxyallyl cycloaddition." Science 362, no. 6414 (November 1, 2018): 564–68. http://dx.doi.org/10.1126/science.aau4821.
Повний текст джерелаLash, Timothy D. "Carbaporphyrins, porphyrin isomers and the legacy of Emanuel Vogel." Journal of Porphyrins and Phthalocyanines 16, no. 05n06 (May 2012): 423–33. http://dx.doi.org/10.1142/s1088424612300017.
Повний текст джерелаMcCombie, Stuart W., Sue-Ing Lin, and Susan F. Vice. "New reactions of hydrazides. Part 1: Directed ortho- and lateral metalation of aromatic carbocyclic and heterocyclic systems." Tetrahedron Letters 40, no. 50 (December 1999): 8767–70. http://dx.doi.org/10.1016/s0040-4039(99)01876-6.
Повний текст джерелаLi, Yang, Jin-Xia Li, Xuan-Hui Ouyang, Qiu-An Wang та Jin-Heng Li. "Manganese-Catalyzed Intermolecular Oxidative Annulation of Alkynes with γ-Vinyl Aldehydes: An Entry to Bridged Carbocyclic Systems". Organic Letters 19, № 22 (27 жовтня 2017): 6172–75. http://dx.doi.org/10.1021/acs.orglett.7b03086.
Повний текст джерелаGómez, Generosa, Hilda Rivera, Isela García, Laura Estévez, and Yagamare Fall. "The furan approach to carbocyclic systems. Synthesis of cyclohexane derivatives from butenolides through an intramolecular Michael addition." Tetrahedron Letters 46, no. 35 (August 2005): 5819–22. http://dx.doi.org/10.1016/j.tetlet.2005.06.137.
Повний текст джерелаDumez, Estelle, Anne-Catherine Durand, Martial Guillaume, Pierre-Yves Roger, Robert Faure, Jean-Marc Pons, Gaëtan Herbette, Jean-Pierre Dulcère, Damien Bonne, and Jean Rodriguez. "Michael Addition Initiated Carbocyclization Sequences with Nitroolefins for the Stereoselective Synthesis of Functionalized Heterocyclic and Carbocyclic Systems." Chemistry - A European Journal 15, no. 45 (October 15, 2009): 12470–88. http://dx.doi.org/10.1002/chem.200901433.
Повний текст джерелаShiota, H., K. Nitta, T. Naito, Y. Mimura, and T. Maruyama. "Clinical evaluation of carbocyclic oxetanocin G eyedrops in the treatment of herpes simplex corneal ulcers." British Journal of Ophthalmology 80, no. 5 (May 1, 1996): 413–15. http://dx.doi.org/10.1136/bjo.80.5.413.
Повний текст джерелаWeinreb, Steven, Wenchun Chao, and Matthew Meketa. "Ring-Closing Metathesis of Vinyl Chlorides for Formation of 5-, 6- and 7-Membered Carbocyclic and Heterocyclic Systems." Synthesis 2004, no. 12 (April 2, 2004): 2058–61. http://dx.doi.org/10.1055/s-2004-822327.
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