Статті в журналах з теми "Symmetric/Asymmetric Catalysis"
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Wang, Xiao-Chen, Zhao-Ying Yang, and Ming Zhang. "Synthesis and Applications of Chiral Bicyclic Bisborane Catalysts." Synthesis 54, no. 06 (November 19, 2021): 1527–36. http://dx.doi.org/10.1055/a-1701-7679.
Повний текст джерелаDesimoni, Giovanni, Giuseppe Faita, and Karl Anker Jørgensen. "C2-Symmetric Chiral Bis(Oxazoline) Ligands in Asymmetric Catalysis." Chemical Reviews 106, no. 9 (September 2006): 3561–651. http://dx.doi.org/10.1021/cr0505324.
Повний текст джерелаHenderson, Alexander S., John F. Bower, and M. Carmen Galan. "Carbohydrate-based N-heterocyclic carbenes for enantioselective catalysis." Org. Biomol. Chem. 12, no. 45 (2014): 9180–83. http://dx.doi.org/10.1039/c4ob02056a.
Повний текст джерелаLitwinienko, Grzegorz, Gino A. DiLabio, and K. U. Ingold. "A theoretical and experimental investigation of some unusual intermolecular hydrogen-bond IR bands — Appearances can be deceptive." Canadian Journal of Chemistry 84, no. 10 (October 1, 2006): 1371–79. http://dx.doi.org/10.1139/v06-097.
Повний текст джерелаRuppel, Joshua V., Xin Cui, Xue Xu та X. Peter Zhang. "Stereoselective intramolecular cyclopropanation of α-diazoacetates via Co(ii)-based metalloradical catalysis". Org. Chem. Front. 1, № 5 (2014): 515–20. http://dx.doi.org/10.1039/c4qo00041b.
Повний текст джерелаCostabile, Chiara, Stefania Pragliola, and Fabia Grisi. "C2-Symmetric N-Heterocyclic Carbenes in Asymmetric Transition-Metal Catalysis." Symmetry 14, no. 8 (August 5, 2022): 1615. http://dx.doi.org/10.3390/sym14081615.
Повний текст джерелаCastillón, Sergio, Carmen Claver, and Yolanda Díaz. "C1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis." Chemical Society Reviews 34, no. 8 (2005): 702. http://dx.doi.org/10.1039/b400361f.
Повний текст джерелаVogl, Erasmus M., Shigeki Matsunaga, Motomu Kanai, Takehiko Iida, and Masakatsu Shibasaki. "Linking BINOL: C2-symmetric ligands for investigations on asymmetric catalysis." Tetrahedron Letters 39, no. 43 (October 1998): 7917–20. http://dx.doi.org/10.1016/s0040-4039(98)01756-0.
Повний текст джерелаAl-Majid, Abdullah M., Brian L. Booth, and Jonnes T. Gomes. "C2-Symmetric Ligands for Asymmetric Catalysis based on Feist's Acid." Journal of Chemical Research, no. 2 (1998): 78–79. http://dx.doi.org/10.1039/a706185d.
Повний текст джерелаvan Slagmaat, Christian A. M. R., Khi Chhay Chou, Lukas Morick, Darya Hadavi, Burgert Blom, and Stefaan M. A. De Wildeman. "Synthesis and Catalytic Application of Knölker-Type Iron Complexes with a Novel Asymmetric Cyclopentadienone Ligand Design." Catalysts 9, no. 10 (September 22, 2019): 790. http://dx.doi.org/10.3390/catal9100790.
Повний текст джерелаLemmens, Lenne J. M., Job A. L. Roodhuizen, Tom F. A. Greef, Albert J. Markvoort, and Luc Brunsveld. "Designed Asymmetric Protein Assembly on a Symmetric Scaffold." Angewandte Chemie International Edition 59, no. 29 (May 18, 2020): 12113–21. http://dx.doi.org/10.1002/anie.202003626.
Повний текст джерелаDesimoni, Giovanni, Giuseppe Faita, and Karl Anker Jørgensen. "Update 1 of:C2-Symmetric Chiral Bis(oxazoline) Ligands in Asymmetric Catalysis." Chemical Reviews 111, no. 11 (November 9, 2011): PR284—PR437. http://dx.doi.org/10.1021/cr100339a.
Повний текст джерелаGenet, Jean Pierre, Angela Marinetti, and Virginie Ratovelomanana-Vidal. "Recent advances in asymmetric catalysis. Synthetic applications to biologically active compounds." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 299–303. http://dx.doi.org/10.1351/pac200173020299.
Повний текст джерелаChelucci, Giorgio. "New chiral C2-symmetric bis(oxazolinylpyridinyl)dioxolane ligands for asymmetric catalysis: palladium catalysed allylic substitution." Tetrahedron: Asymmetry 8, no. 16 (August 1997): 2667–70. http://dx.doi.org/10.1016/s0957-4166(97)00318-2.
Повний текст джерелаPedersen, Stephan K., Kristina Eriksen, and Michael Pittelkow. "Symmetric, Unsymmetrical, and Asymmetric [7]‐, [10]‐, and [13]Helicenes." Angewandte Chemie International Edition 58, no. 51 (November 6, 2019): 18419–23. http://dx.doi.org/10.1002/anie.201910214.
Повний текст джерелаKumari, Beena, Surya Pratap Singh, Ranga Santosh, Arnab Dutta, Sairam S. Mallajosyula, Subhas Ghosal, and Sriram Kanvah. "Branching effect on triphenylamine-CF3 cyanostilbenes: enhanced emission and aggregation in water." New Journal of Chemistry 43, no. 10 (2019): 4106–15. http://dx.doi.org/10.1039/c8nj05907a.
Повний текст джерелаSnider, Barry B., James F. Grabowski, Roger W. Alder, Bruce M. Foxman, and Lin Yang. "Synthesis of a hindered C2-symmetric hydrazine and diamine by a crisscross cycloaddition of citronellal azine." Canadian Journal of Chemistry 84, no. 10 (October 1, 2006): 1242–49. http://dx.doi.org/10.1139/v06-084.
Повний текст джерелаBerkessel, Albrecht, Michael Schröder, Christoph A. Sklorz, Stefania Tabanella, Nadine Vogl, Johann Lex, and Jörg M. Neudörfl. "Enantioselective Synthesis of DIANANE, a NovelC2-Symmetric Chiral Diamine for Asymmetric Catalysis†." Journal of Organic Chemistry 69, no. 9 (April 2004): 3050–56. http://dx.doi.org/10.1021/jo035841d.
Повний текст джерелаReetz, Manfred T., and Andreas Gosberg. "New non-C2-symmetric phosphine-phosphonites as ligands in asymmetric metal catalysis." Tetrahedron: Asymmetry 10, no. 11 (June 1999): 2129–37. http://dx.doi.org/10.1016/s0957-4166(99)00215-3.
Повний текст джерелаPowell, Mark T., Alexander M. Porte, and Kevin Burgess. "On the efficacy of propeller-shaped, C3-symmetric triarylphosphines in asymmetric catalysis." Chemical Communications, no. 19 (1998): 2161–62. http://dx.doi.org/10.1039/a806811i.
Повний текст джерелаVOGL, E. M., S. MATSUNAGA, M. KANAI, T. IIDA, and M. SHIBASAKI. "ChemInform Abstract: Linking BINOL: C2-Symmetric Ligands for Investigations on Asymmetric Catalysis." ChemInform 30, no. 1 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199901046.
Повний текст джерелаLaufer, Radoslaw, Ulrich Veith, Nicholas J. Taylor, and Victor Snieckus. "(–)-Sparteine-mediated stereoselective directed ortho metalation of ferrocene diamides." Canadian Journal of Chemistry 84, no. 2 (February 1, 2006): 356–69. http://dx.doi.org/10.1139/v06-008.
Повний текст джерелаPfaltz, Andreas, Hans Adolfsson, Kenneth Wärnmark, Kari Aasbø, Martti Klinga, and Antonio Romerosa. "Design of Chiral Ligands for Asymmetric Catalysis: from C2-Symmetric Semicorrins and Bisoxazolines to Non-Symmetric Phosphinooxazolines." Acta Chemica Scandinavica 50 (1996): 189–94. http://dx.doi.org/10.3891/acta.chem.scand.50-0189.
Повний текст джерелаNarine, Arun A., and Peter D. Wilson. "Synthesis and evaluation of 7-hydroxyindan-1-one-derived chiral auxiliaries." Canadian Journal of Chemistry 83, no. 5 (May 1, 2005): 413–19. http://dx.doi.org/10.1139/v05-052.
Повний текст джерелаOhshima, Takashi, Takahito Kawabata, Yosuke Takeuchi, Takahiro Kakinuma, Takanori Iwasaki, Takayuki Yonezawa, Hajime Murakami, Hisao Nishiyama та Kazushi Mashima. "C1-Symmetric Rh/Phebox-Catalyzed Asymmetric Alkynylation of α-Ketoesters". Angewandte Chemie International Edition 50, № 28 (30 травня 2011): 6296–300. http://dx.doi.org/10.1002/anie.201100252.
Повний текст джерелаKisszékelyi, Péter, Zsuzsanna Fehér, Sándor Nagy, Péter Bagi, Petra Kozma, Zsófia Garádi, Miklós Dékány, Péter Huszthy, Béla Mátravölgyi, and József Kupai. "Synthesis of C3-Symmetric Cinchona-Based Organocatalysts and Their Applications in Asymmetric Michael and Friedel–Crafts Reactions." Symmetry 13, no. 3 (March 23, 2021): 521. http://dx.doi.org/10.3390/sym13030521.
Повний текст джерелаGuiry, Patrick, and Steven O’Reilly. "Recent Applications of C 1-Symmetric Bis(oxazoline)-Containing Ligands in Asymmetric Catalysis." Synthesis 46, no. 06 (February 19, 2014): 722–39. http://dx.doi.org/10.1055/s-0033-1340829.
Повний текст джерелаAL-MAJID, A. M., B. L. BOOTH, and J. T. GOMES. "ChemInform Abstract: C2-Symmetric Ligands for Asymmetric Catalysis Based on Feist′s Acid." ChemInform 30, no. 10 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199910081.
Повний текст джерелаTrost, Barry M., Zhengying Pan, Jorge Zambrano, and Christof Kujat. "Polymer-SupportedC2-Symmetric Ligands for Palladium-Catalyzed Asymmetric Allylic Alkylation Reactions." Angewandte Chemie International Edition 41, no. 24 (December 16, 2002): 4691–93. http://dx.doi.org/10.1002/anie.200290018.
Повний текст джерелаBao, Changjiang, Yanwei Li, Yanhui Li, Zhenjun Si, Yanru Zhang, Changshun Chen, Lei Wang, and Qian Duan. "A series of asymmetric and symmetric porphyrin derivatives: one-pot synthesis, nonlinear optical and optical limiting properties." New Journal of Chemistry 45, no. 35 (2021): 16030–38. http://dx.doi.org/10.1039/d1nj02632a.
Повний текст джерелаGreencorn, David J., Victoria M. Sandre, Emily K. Piggott, Michael R. Hillier, A. James Mitchell, Taryn M. Reid, Michael J. McAlduff, Kulbir Singh, and D. Gerrard Marangoni. "Asymmetric cationic gemini surfactants: an improved synthetic procedure and the micellar and surface properties of a homologous series in the presence of simple salts." Canadian Journal of Chemistry 96, no. 7 (July 2018): 672–80. http://dx.doi.org/10.1139/cjc-2017-0676.
Повний текст джерелаKarunaratne, Veranja, and David Dolphin. "Oxidation of 2-methylpyrroles with perchlorinated iron(III) metalloporphyrin catalysts: a versatile synthesis of symmetric and asymmetric dipyrromethanes." Canadian Journal of Chemistry 76, no. 10 (October 1, 1998): 1467–73. http://dx.doi.org/10.1139/v98-190.
Повний текст джерелаPFALTZ, A. "ChemInform Abstract: Design of Chiral Ligands for Asymmetric Catalysis: From C2-Symmetric Semicorrins and Bisoxazolines to Non-Symmetric Phosphinooxazolines." ChemInform 27, no. 29 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199629287.
Повний текст джерелаAromí, Guillem, Paula Carrero Berzal, Patrick Gamez, Olivier Roubeau, Huub Kooijman, Anthony L. Spek, Willem L. Driessen, and Jan Reedijk. "A Unique Asymmetric [Mn] Triple-Stranded Helicate from a Symmetric Pentadentate Ligand." Angewandte Chemie International Edition 40, no. 18 (September 17, 2001): 3444–46. http://dx.doi.org/10.1002/1521-3773(20010917)40:18<3444::aid-anie3444>3.0.co;2-q.
Повний текст джерелаKałuża, Zbigniew, Rafał Ćwiek, Mirosław Dygas, and Przemysław Kalicki. "Diamine Ligands for Asymmetric Catalysis: Facile Synthesis of C2-Symmetric Piperazines from Seebach’s Oxazolidinone." Synlett 25, no. 13 (July 8, 2014): 1883–87. http://dx.doi.org/10.1055/s-0034-1378341.
Повний текст джерелаDesimoni, Giovanni, Giuseppe Faita, and Karl Anker Joergensen. "ChemInform Abstract: Update 1 Of: C2-Symmetric Chiral Bis(oxazoline) Ligands in Asymmetric Catalysis." ChemInform 44, no. 52 (December 5, 2013): no. http://dx.doi.org/10.1002/chin.201352250.
Повний текст джерелаPOWELL, M. T., A. M. PORTE, and K. BURGESS. "ChemInform Abstract: On the Efficacy of Propeller-Shaped, C3-Symmetric Triarylphosphines in Asymmetric Catalysis." ChemInform 30, no. 2 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199902114.
Повний текст джерелаReetz, Manfred T., and Andreas Gosberg. "ChemInform Abstract: New Non-C2-Symmetric Phosphine-Phosphonites as Ligands in Asymmetric Metal Catalysis." ChemInform 30, no. 48 (June 12, 2010): no. http://dx.doi.org/10.1002/chin.199948039.
Повний текст джерелаNakagawa, Hiroshi, Yoshihisa Sei, Kentaro Yamaguchi, Tetsuo Nagano, and Tsunehiko Higuchi. "Catalytic and asymmetric epoxidation by novel D4-symmetric chiral porphyrin derived from C2-symmetric diol." Journal of Molecular Catalysis A: Chemical 219, no. 2 (September 2004): 221–26. http://dx.doi.org/10.1016/j.molcata.2004.05.026.
Повний текст джерелаGarcía-García, F. R., and K. Li. "New catalytic reactors prepared from symmetric and asymmetric ceramic hollow fibres." Applied Catalysis A: General 456 (April 2013): 1–10. http://dx.doi.org/10.1016/j.apcata.2013.01.031.
Повний текст джерелаLeón, Félix, Javier Francos, Joaquín López-Serrano, Sergio E. García-Garrido, Victorio Cadierno, and Antonio Pizzano. "Double asymmetric hydrogenation of conjugated dienes: a self-breeding chirality route for C2 symmetric 1,4-diols." Chemical Communications 55, no. 6 (2019): 786–89. http://dx.doi.org/10.1039/c8cc09391a.
Повний текст джерелаYang, Gink N., Parinaz Ahangar, Xanthe L. Strudwick, Zlatko Kopecki, and Allison J. Cowin. "Overexpression of Flii during Murine Embryonic Development Increases Symmetrical Division of Epidermal Progenitor Cells." International Journal of Molecular Sciences 22, no. 15 (July 30, 2021): 8235. http://dx.doi.org/10.3390/ijms22158235.
Повний текст джерелаHeinz, Benjamin, Moritz Balkenhohl, and Paul Knochel. "Thiolation of Pyridine-2-sulfonamides using Magnesium Thiolates." Synthesis 51, no. 23 (September 3, 2019): 4452–62. http://dx.doi.org/10.1055/s-0039-1690199.
Повний текст джерелаWang, Zhi-Xian, Susie M. Miller, Oren P. Anderson, and Yian Shi. "ChemInform Abstract: A Class of C2 and Pseudo C2 Symmetric Ketone Catalysts for Asymmetric Epoxidation. Conformational Effect on Catalysis." ChemInform 31, no. 1 (June 12, 2010): no. http://dx.doi.org/10.1002/chin.200001128.
Повний текст джерелаDube, Edith, Njemuwa Nwaji, John Mack, and Tebello Nyokong. "The photophysicochemical behavior of symmetric and asymmetric zinc phthalocyanines, surface assembled onto gold nanotriangles." New Journal of Chemistry 42, no. 17 (2018): 14290–99. http://dx.doi.org/10.1039/c8nj02746c.
Повний текст джерелаEno, Meredith S., Alexander Lu, and James P. Morken. "Nickel-Catalyzed Asymmetric Kumada Cross-Coupling of Symmetric Cyclic Sulfates." Journal of the American Chemical Society 138, no. 25 (June 16, 2016): 7824–27. http://dx.doi.org/10.1021/jacs.6b03384.
Повний текст джерелаWakchaure, Vijay N., and Benjamin List. "Catalytic Asymmetric Reductive Condensation of N-H Imines: Synthesis ofC2-Symmetric Secondary Amines." Angewandte Chemie International Edition 55, no. 51 (November 22, 2016): 15775–78. http://dx.doi.org/10.1002/anie.201608329.
Повний текст джерелаGendrineau, Thomas, Olivier Chuzel, Hendrik Eijsberg, Jean-Pierre Genet, and Sylvain Darses. "C1-Symmetric Monosubstituted Chiral Diene Ligands in Asymmetric Rhodium-Catalyzed 1,4-Addition Reactions." Angewandte Chemie International Edition 47, no. 40 (September 22, 2008): 7669–72. http://dx.doi.org/10.1002/anie.200803230.
Повний текст джерелаLangner, Martin, and Carsten Bolm. "C1-Symmetric Sulfoximines as Ligands in Copper-Catalyzed Asymmetric Mukaiyama-Type Aldol Reactions." Angewandte Chemie International Edition 43, no. 44 (November 12, 2004): 5984–87. http://dx.doi.org/10.1002/anie.200460953.
Повний текст джерелаMorimoto, Yoshiki, Takamasa Kinoshita, and Toshiyuki Iwai. "Asymmetric total synthesis of highly symmetric squalene-derived cytotoxic polyethers." Chirality 14, no. 7 (2002): 578–86. http://dx.doi.org/10.1002/chir.10083.
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