Статті в журналах з теми "Endo-exo selectivity"
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Ward, Dale E., and Yuanzhu Gai. "Lewis acid mediated Diels–Alder reactions of 2H-thiopyrans." Canadian Journal of Chemistry 70, no. 10 (October 1, 1992): 2627–34. http://dx.doi.org/10.1139/v92-331.
Повний текст джерелаShivanyuk, Alexander, Andrii Gerasov, Rodion Boiko, Grygoriy Dolgonos, Aleksandr Mandzhulo, Volodymyr Fetyukhin, and Oleg Lukin. "Tropane-Based Dispirocyclic Oxiranes and Spirocyclic Ketones." Synthesis 54, no. 03 (December 6, 2021): 723–31. http://dx.doi.org/10.1055/s-0040-1719848.
Повний текст джерелаOkuda, Yasuhiro, Robert K. Szilagyi, Seiji Mori, and Yasushi Nishihara. "The origin of exo-selectivity in methyl cyanoformate addition onto the CC bond of norbornene in Pd-catalyzed cyanoesterification." Dalton Trans. 43, no. 25 (2014): 9537–48. http://dx.doi.org/10.1039/c4dt00839a.
Повний текст джерелаInfante, Genesis, and Sara Eisler. "Accessing pyrrolones and pyridinones: controlling 5-exo and 6-endo ring closures in heterocyclic alkynylamides." Canadian Journal of Chemistry 95, no. 4 (April 2017): 415–23. http://dx.doi.org/10.1139/cjc-2016-0524.
Повний текст джерелаLegnani, Laura, Salvatore V. Giofré, Daniela Iannazzo, Consuelo Celesti, Lucia Veltri, and Maria Assunta Chiacchio. "Chemoselective Oxidation of Isoxazolidines with Ruthenium Tetroxide: A Successful Intertwining of Combined Theoretical and Experimental Data." Molecules 27, no. 17 (August 24, 2022): 5390. http://dx.doi.org/10.3390/molecules27175390.
Повний текст джерелаTamilmani, V., C. A. Daul, and P. Venuvanalingam. "Electrostatic control on endo/exo selectivity in ionic cycloaddition." Chemical Physics Letters 416, no. 4-6 (December 2005): 354–57. http://dx.doi.org/10.1016/j.cplett.2005.09.120.
Повний текст джерелаSolans-Monfort, Xavier. "DFT study on the reaction mechanism of the ring closing enyne metathesis (RCEYM) catalyzed by molybdenum alkylidene complexes." Dalton Trans. 43, no. 11 (2014): 4573–86. http://dx.doi.org/10.1039/c3dt53242a.
Повний текст джерелаİşleyen, Alper, Tuğmac Sayraç, and Özdemir Doğan. "Boron Trifluoride Mediated Addition of Nucleophiles to endo- and exo-Substituted Norbornene Derivatives." Zeitschrift für Naturforschung B 59, no. 1 (January 1, 2004): 109–18. http://dx.doi.org/10.1515/znb-2004-0116.
Повний текст джерелаGerasov, Andrii, Grygoriy A. Dolgonos, Aleksandr Yu Mandzhulo, Alexey Ryabitsky, Volodymyr Fetyukhin, Oleg Lukin, and Alexander Shivanyuk. "Selective Synthesis of exo-Spiro[2′,2′-difluorocyclopropane-3′,2′-tropanes]." Synthesis 52, no. 07 (January 2, 2020): 1015–24. http://dx.doi.org/10.1055/s-0039-1691560.
Повний текст джерелаGosse, Tammy L., and Raymond A. Poirier. "Exo selectivity and the effect of disubstitution in the DielsAlder reactions of butadiene with 3,3-disubstituted cyclopropenes." Canadian Journal of Chemistry 82, no. 11 (November 1, 2004): 1589–96. http://dx.doi.org/10.1139/v04-115.
Повний текст джерелаFišera, Lubor, Vladimír Oremus, Ladislav Štibrányi, Hans-Joachim Timpe, and Alena Máťušová. "Photo-induced rearrangement of isoxazolines - A pathway to 2,4,5,8-tetrahydro-1,3-dioxa-5-azocine derivatives." Collection of Czechoslovak Chemical Communications 50, no. 9 (1985): 1982–93. http://dx.doi.org/10.1135/cccc19851982.
Повний текст джерелаMinuti, Lucio, Roberta Selvaggi, Aldo Taticchi, Ming Guo, and Ernest Wenkert. "Diels–Alder reactions of bicyclic, heteroannular dienones." Canadian Journal of Chemistry 70, no. 5 (May 1, 1992): 1481–85. http://dx.doi.org/10.1139/v92-183.
Повний текст джерелаYan, Shihai, Do-Hyun Ryu, and Jin-Yong Lee. "Origin of Exo/Endo Selectivity in the Intramolecular Diels-Alder Reaction." Bulletin of the Korean Chemical Society 31, no. 9 (September 20, 2010): 2527–30. http://dx.doi.org/10.5012/bkcs.2010.31.9.2527.
Повний текст джерелаBatllori, Rosa, Josep Font, Montserrat Monsalvatje, Rosa M. Ortuño, and Francisco Sanchez-Ferrando. "Diels-alder cycloadditions of chiral butenolides with cyclopentadiene: endo/exo selectivity." Tetrahedron 45, no. 6 (January 1989): 1833–38. http://dx.doi.org/10.1016/s0040-4020(01)80048-x.
Повний текст джерелаVelez, Caroline, Brian Doherty, and Orlando Acevedo. "Accurate Diels-Alder Energies and Endo Selectivity in Ionic Liquids Using the OPLS-VSIL Force Field." International Journal of Molecular Sciences 21, no. 4 (February 11, 2020): 1190. http://dx.doi.org/10.3390/ijms21041190.
Повний текст джерелаSuárez, D., and J. A. Sordo. "On the origin of the endo/exo selectivity in Diels–Alder reactions." Chemical Communications, no. 3 (1998): 385–86. http://dx.doi.org/10.1039/a707086a.
Повний текст джерелаWałejko, Piotr, Michał Dąbrowski, Lech Szczepaniak, Jacek W. Morzycki, and Stanisław Witkowski. "Stereochemistry of ring-opening/cross metathesis reactions of exo- and endo-7-oxabicyclo[2.2.1]hept-5-ene-2-carbonitriles with allyl alcohol and allyl acetate." Beilstein Journal of Organic Chemistry 11 (October 13, 2015): 1893–901. http://dx.doi.org/10.3762/bjoc.11.204.
Повний текст джерелаCainelli, Gianfranco, Paola Galletti, Daria Giacomini, and Arianna Quintavalla. "Dynamic solvation effects on the endo/exo selectivity of the Diels–Alder reaction." Tetrahedron Letters 44, no. 1 (January 2003): 93–96. http://dx.doi.org/10.1016/s0040-4039(02)02477-2.
Повний текст джерелаZimmerman, Howard E., and Linus W. Linder. "Enhanced endo-exo selectivity in the stereochemistry of ketonization of enols. Part 201." Journal of Organic Chemistry 50, no. 10 (May 1985): 1637–46. http://dx.doi.org/10.1021/jo00210a016.
Повний текст джерелаSustmann, Reiner, Willi Sicking, Hélène Lamy-Schelkens, and Léon Ghosez. "endo/exo selectivity in cycloadditions of 2,6-bis-silyloxy-3,4-dihydropyridine with methylacrylate." Tetrahedron Letters 32, no. 11 (March 1991): 1401–4. http://dx.doi.org/10.1016/0040-4039(91)80341-3.
Повний текст джерелаMerouani, Hafida, Christophe Morell, Nadia Ouddai, and Henry Chermette. "DFT study of the stereo-selectivity of oxygenated heterocycles from 10 to 12 links." Canadian Journal of Chemistry 91, no. 9 (September 2013): 811–20. http://dx.doi.org/10.1139/cjc-2012-0521.
Повний текст джерелаWerstiuk, Nick Henry, та Chandra Deo Roy. "Experimental and AM1 calculational studies of the deprotonation of bicyclo[2.2.2]octane-2,5-dione and bicyclo[2.2.2]octane-2,6-dione: a study of homoconjugation, inductive, and steric effects on the rates and diastereoselectivities of α enolization". Canadian Journal of Chemistry 73, № 3 (1 березня 1995): 460–63. http://dx.doi.org/10.1139/v95-060.
Повний текст джерелаSchwarz, Joseph, and Helmut Schwarz. "exo/endo-Selectivity in the Reaction of ?Bare? FeO+ with Bicyclo[2.2.1]heptane (Norbornane)." Helvetica Chimica Acta 78, no. 4 (June 28, 1995): 1013–19. http://dx.doi.org/10.1002/hlca.19950780423.
Повний текст джерелаMeir, Rinat, Hui Chen, Wenzhen Lai, and Sason Shaik. "Corrigendum: Oriented Electric Fields Accelerate Diels–Alder Reactions and Control the endo / exo Selectivity." ChemPhysChem 21, no. 15 (August 4, 2020): 1737. http://dx.doi.org/10.1002/cphc.201900495.
Повний текст джерелаSUSTMANN, R., W. SICKING, H. LAMY-SCHELKENS, and L. GHOSEZ. "ChemInform Abstract: endo/exo-Selectivity in Cycloadditions of 2,6-Bissilyloxy-3,4- dihydropyridine with Methylacrylate." ChemInform 23, no. 2 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199202085.
Повний текст джерелаHooper, Joel F., Jonathan M. White, and Andrew B. Holmes. "Development of the Claisen Rearrangement/Organocatalytic Diels-Alder Approach for the Synthesis of Eunicellins." Australian Journal of Chemistry 67, no. 9 (2014): 1189. http://dx.doi.org/10.1071/ch14030.
Повний текст джерелаŠmit, Biljana M., Radoslav Z. Pavlović, Dejan A. Milenković, and Zoran S. Marković. "Mechanism, kinetics and selectivity of selenocyclization of 5-alkenylhydantoins: an experimental and computational study." Beilstein Journal of Organic Chemistry 11 (October 7, 2015): 1865–75. http://dx.doi.org/10.3762/bjoc.11.200.
Повний текст джерелаParvez, M., A. Rauk, T. S. Sorensen, and F. Sun. "Structure reassignment of the major isomer from the Diels-Alder reaction of acryloyl chloride and 4,5,6,6a-tetrahydropentalene." Canadian Journal of Chemistry 76, no. 9 (September 1, 1998): 1289–93. http://dx.doi.org/10.1139/v98-168.
Повний текст джерелаMcCleary, Barry V., Lucie M. J. Charmier, Vincent A. McKie, Ciara McLoughlin, and Artur Rogowski. "Determination of Fructan (Inulin, FOS, Levan, and Branched Fructan) in Animal Food (Animal Feed, Pet Food, and Ingredients): Single-Laboratory Validation, First Action 2018.07." Journal of AOAC INTERNATIONAL 102, no. 3 (May 1, 2019): 883–92. http://dx.doi.org/10.5740/jaoacint.18-0330.
Повний текст джерелаSato, Michio, Shinji Kishimoto, Mamoru Yokoyama, Cooper S. Jamieson, Kazuto Narita, Naoya Maeda, Kodai Hara, et al. "Catalytic mechanism and endo-to-exo selectivity reversion of an octalin-forming natural Diels–Alderase." Nature Catalysis 4, no. 3 (March 2021): 223–32. http://dx.doi.org/10.1038/s41929-021-00577-2.
Повний текст джерелаNiwayama, Satomi, Hanjoung Cho, Masoud Zabet-Moghaddam, and Bruce R. Whittlesey. "Remote Exo/Endo Selectivity in Selective Monohydrolysis of Dialkyl Bicyclo[2.2.1]heptane-2,3-dicarboxylate Derivatives." Journal of Organic Chemistry 75, no. 11 (June 4, 2010): 3775–80. http://dx.doi.org/10.1021/jo100564e.
Повний текст джерелаHa, Jae Du, Chul Hyun Kang, Kenneth A. Belmore, and Jin Kun Cha. "Diels−Alder Reactions of 2-(N-Acylamino)-1,3-dienes. Atypical Regioselectivity and Endo/Exo Selectivity." Journal of Organic Chemistry 63, no. 12 (June 1998): 3810–11. http://dx.doi.org/10.1021/jo980593k.
Повний текст джерелаKeseru, G. "Theoretical study on the 5-exo/6-endo selectivity in the cyclization of electrophilic radicals." Journal of Molecular Structure: THEOCHEM 392, no. 1 (March 31, 1997): 95–99. http://dx.doi.org/10.1016/s0166-1280(96)04870-1.
Повний текст джерелаKeseru, György M., László Toke, Zoltán Hell, Zsuzsanna M. Jászay, Imre Petneházy, and László Korecz. "Theoretical study on the 5-exo/6-endo selectivity in the cyclization of electrophilic radicals." Journal of Molecular Structure: THEOCHEM 392 (March 1997): 95–99. http://dx.doi.org/10.1016/s0166-1280(97)90381-x.
Повний текст джерелаHooper, Joel F., Natalie C. James, Esra Bozkurt, Viktorya Aviyente, Jonathan M. White, Mareike C. Holland, Ryan Gilmour, Andrew B. Holmes, and K. N. Houk. "Medium-Ring Effects on the Endo/Exo Selectivity of the Organocatalytic Intramolecular Diels–Alder Reaction." Journal of Organic Chemistry 80, no. 24 (November 30, 2015): 12058–75. http://dx.doi.org/10.1021/acs.joc.5b02037.
Повний текст джерелаAlonzo, Daniel, Vicen¢ Branchadell, Josep Font, Antonio Oliva, Rosa M. Ortuño, and Francisco Sánchez-Ferrando. "5-Methylene-2(5H)-furanone in Diels-Alder reactions with cyclic dienes: endo/exo selectivity." Tetrahedron 46, no. 12 (1990): 4371–78. http://dx.doi.org/10.1016/s0040-4020(01)86771-5.
Повний текст джерелаLarrañaga, Olatz, та Abel de Cózar. "Effect of an α-Methyl Substituent on the Dienophile on Diels-Alder endo :exo Selectivity". ChemistryOpen 8, № 1 (січень 2019): 49–57. http://dx.doi.org/10.1002/open.201800237.
Повний текст джерелаBarešić, Luka, Davor Margetić, and Zoran Glasovac. "Cycloaddition of Thiourea- and Guanidine-Substituted Furans to Dienophiles: A Comparison of the Environmentally-Friendly Methods." Chemistry Proceedings 3, no. 1 (November 14, 2020): 57. http://dx.doi.org/10.3390/ecsoc-24-08380.
Повний текст джерелаNiwayama, Satomi, and Yoshikazu Hiraga. "New exo/endo selectivity observed in monohydrolysis of dialkyl bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylates." Tetrahedron Letters 44, no. 47 (November 2003): 8567–70. http://dx.doi.org/10.1016/j.tetlet.2003.09.131.
Повний текст джерелаYates, Peter, Anabela Gomes, D. Jean Burnell, Dong Dao Cong, and Jeffery F. Sawyer. "Some 6,6-disubstituted 2,4-cyclohexadien-1-ones and the facial selectivity in their Diels–Alder reactions with dimethyl acetylenedicarboxylate." Canadian Journal of Chemistry 67, no. 1 (January 1, 1989): 37–47. http://dx.doi.org/10.1139/v89-007.
Повний текст джерелаLang, Yanmin, Mei Zhang, Yang Cao, and Genping Huang. "Mechanism and origins of the directing group-controlled endo- versus exo-selectivity of iridium-catalysed intramolecular hydroalkenylation of 1,1-disubstituted alkenes." Chemical Communications 54, no. 21 (2018): 2678–81. http://dx.doi.org/10.1039/c8cc00074c.
Повний текст джерелаLi, Zhenghua, Amit Kumar, Sunil K. Sharma, Virinder S. Parmar, and Erik V. Van der Eycken. "Catalyst-controlled exo/endo selectivity in a post-Ugi intramolecular hydroarylation: synthesis of pyrrolopyridinones, pyrroloazepinones, and benzothienopyridines." Tetrahedron 71, no. 21 (May 2015): 3333–42. http://dx.doi.org/10.1016/j.tet.2015.03.103.
Повний текст джерелаSodupe, Mariona, Raphael Rios, Vicenç Branchadell, Tony Nicholas, Antonio Oliva, and J. J. Dannenberg. "A Theoretical Study of the Endo/Exo Selectivity of the Diels−Alder Reaction between Cyclopropene and Butadiene." Journal of the American Chemical Society 119, no. 18 (May 1997): 4232–38. http://dx.doi.org/10.1021/ja9628260.
Повний текст джерелаHA, J. D., C. H. KANG, K. A. BELMORE, and J. K. CHA. "ChemInform Abstract: Diels-Alder Reactions of 2-(N-Acylamino)-1,3-dienes. Atypical Regioselectivity and endo/exo Selectivity." ChemInform 29, no. 45 (June 19, 2010): no. http://dx.doi.org/10.1002/chin.199845155.
Повний текст джерелаPenín, Lucía, Matteo Gigli, Federica Sabuzi, Valentín Santos, Pierluca Galloni, Valeria Conte, Juan Carlos Parajó, Heiko Lange, and Claudia Crestini. "Biomimetic Vanadate and Molybdate Systems for Oxidative Upgrading of Iono- and Organosolv Hard- and Softwood Lignins." Processes 8, no. 9 (September 16, 2020): 1161. http://dx.doi.org/10.3390/pr8091161.
Повний текст джерелаSchlachter, Ingo, Jochen Mattay, Josef Suer, Udo Höweler, Gudrun Würthwein, and Ernst-Ulrich Würthwein. "Combined quantum chemical and MM-approach to the endo/exo selectivity of diels-alder reactions in polar media." Tetrahedron 53, no. 1 (January 1997): 119–32. http://dx.doi.org/10.1016/s0040-4020(96)00957-x.
Повний текст джерелаDi Valentin, Cristiana, Mauro Freccero, Mirko Sarzi-Amadè, and Riccardo Zanaletti. "Reactivity and endo–exo Selectivity in Diels–Alder Reaction of o-Quinodimethanes. An Experimental and DFT Computational Study." Tetrahedron 56, no. 16 (April 2000): 2547–59. http://dx.doi.org/10.1016/s0040-4020(00)00126-5.
Повний текст джерелаTakeda, Kei, Ikuhiro Imaoka та Eiichi Yoshii. "Diels-Alder reaction of α-substituted acrylates and α-(methylene)lactones: Conformation of dienophiles and endo/exo selectivity". Tetrahedron 50, № 37 (січень 1994): 10839–48. http://dx.doi.org/10.1016/s0040-4020(01)85696-9.
Повний текст джерелаMa, Mengtao, Ruifeng Lu, Sumod A. Pullarkat, Weiqiao Deng, and Pak-Hing Leung. "Steric effects on the control of endo/exo-selectivity in the asymmetric cycloaddition reaction of 3,4-dimethyl-1-phenylarsole." Dalton Transactions 39, no. 23 (2010): 5453. http://dx.doi.org/10.1039/b924613d.
Повний текст джерелаLi, Zhenghua, Amit Kumar, Sunil K. Sharma, Virinder S. Parmar, and Erik V. Van der Eycken. "ChemInform Abstract: Catalyst-Controlled exo/endo Selectivity in a Post-Ugi Intramolecular Hydroarylation: Synthesis of Pyrrolopyridinones, Pyrroloazepinones, and Benzothienopyridines." ChemInform 46, no. 37 (August 27, 2015): no. http://dx.doi.org/10.1002/chin.201537035.
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