Artigos de revistas sobre o tema "P-Stereogenic catalysts"
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Błaszczyk, Jarosław, Bogdan Bujnicki, Patrycja Pokora-Sobczak, Grażyna Mielniczak, Lesław Sieroń, Piotr Kiełbasiński e Józef Drabowicz. "New Optically Active tert-Butylarylthiophosphinic Acids and Their Selenium Analogues as the Potential Synthons of Supramolecular Organometallic Complexes: Syntheses and Crystallographic Structure Determination". Molecules 28, n.º 11 (24 de maio de 2023): 4298. http://dx.doi.org/10.3390/molecules28114298.
Texto completo da fonteHan, Zhengxu S., Hao Wu, Bo Qu, Yuwen Wang, Ling Wu, Li Zhang, Yibo Xu et al. "New class of P-stereogenic chiral Brønsted acid catalysts derived from chiral phosphinamides". Tetrahedron Letters 60, n.º 28 (julho de 2019): 1834–37. http://dx.doi.org/10.1016/j.tetlet.2019.06.013.
Texto completo da fontevon Münchow, Tristan, Suman Dana, Yang Xu, Binbin Yuan e Lutz Ackermann. "Enantioselective electrochemical cobalt-catalyzed aryl C–H activation reactions". Science 379, n.º 6636 (10 de março de 2023): 1036–42. http://dx.doi.org/10.1126/science.adg2866.
Texto completo da fonteChan, Vincent S., Melanie Chiu, Robert G. Bergman e F. Dean Toste. "Development of Ruthenium Catalysts for the Enantioselective Synthesis of P-Stereogenic Phosphines via Nucleophilic Phosphido Intermediates". Journal of the American Chemical Society 131, n.º 16 (29 de abril de 2009): 6021–32. http://dx.doi.org/10.1021/ja9014887.
Texto completo da fonteGladiali, Serafino, Serenella Medici, Giovanna Pirri, Sonia Pulacchini e Davide Fabbri. "BINAPS - An axially chiral P,S-heterodonor ligand for asymmetric catalysis based on binaphthalene backbone". Canadian Journal of Chemistry 79, n.º 5-6 (1 de maio de 2001): 670–78. http://dx.doi.org/10.1139/v01-041.
Texto completo da fonteBiosca, Maria, Ernest Salomó, Pol de la Cruz-Sánchez, Antoni Riera, Xavier Verdaguer, Oscar Pàmies e Montserrat Diéguez. "Extending the Substrate Scope in the Hydrogenation of Unfunctionalized Tetrasubstituted Olefins with Ir-P Stereogenic Aminophosphine–Oxazoline Catalysts". Organic Letters 21, n.º 3 (16 de janeiro de 2019): 807–11. http://dx.doi.org/10.1021/acs.orglett.8b04084.
Texto completo da fonteBagi, Péter, Réka Herbay, Gábor Györke, Péter Pongrácz, László Kollár, István Timári, László Drahos e György Keglevich. "Preparation of Palladium(II) Complexes of 1-substituted-3-phospholene Ligands and their Evaluation as Catalysts in Hydroalkoxycarbonylation". Current Organic Chemistry 23, n.º 25 (14 de janeiro de 2020): 2873–79. http://dx.doi.org/10.2174/1385272823666191204151311.
Texto completo da fonteHuber, Raffael, Alessandro Passera, Erik Gubler e Antonio Mezzetti. "P-Stereogenic PN(H)P Iron(II) Catalysts for the Asymmetric Hydrogenation of Ketones: The Importance of Non-Covalent Interactions in Rational Ligand Design by Computation". Advanced Synthesis & Catalysis 360, n.º 15 (22 de junho de 2018): 2900–2913. http://dx.doi.org/10.1002/adsc.201800433.
Texto completo da fonteNuman, Ahmed, e Matthew Brichacek. "Asymmetric Synthesis of Stereogenic Phosphorus P(V) Centers Using Chiral Nucleophilic Catalysis". Molecules 26, n.º 12 (15 de junho de 2021): 3661. http://dx.doi.org/10.3390/molecules26123661.
Texto completo da fonteFunk, Michael A. "A P catalyst for stereogenic P(III)". Science 371, n.º 6530 (11 de fevereiro de 2021): 687.5–687. http://dx.doi.org/10.1126/science.371.6530.687-e.
Texto completo da fonteXiang, Yijun, Qianyi Ge, Shulei Wu, Xing Zheng e Zehua Yang. "Synthesis and application in asymmetric catalysis of P-stereogenic pincer–metal complexes". RSC Advances 10, n.º 16 (2020): 9563–78. http://dx.doi.org/10.1039/d0ra00377h.
Texto completo da fonteXie, Xiaoxiao, Sanliang Li, Qiaoyu Chen, Hao Guo, Junfeng Yang e Junliang Zhang. "Synthesis and application of novel P-chiral monophosphorus ligands". Organic Chemistry Frontiers 9, n.º 6 (2022): 1589–92. http://dx.doi.org/10.1039/d1qo01819a.
Texto completo da fonteSchwenk, R., e A. Togni. "P-Trifluoromethyl ligands derived from Josiphos in the Ir-catalysed hydrogenation of 3,4-dihydroisoquinoline hydrochlorides". Dalton Transactions 44, n.º 45 (2015): 19566–75. http://dx.doi.org/10.1039/c5dt02019k.
Texto completo da fonteRojo, Pep, Antoni Riera e Xavier Verdaguer. "Bulky P-stereogenic ligands. A success story in asymmetric catalysis". Coordination Chemistry Reviews 489 (agosto de 2023): 215192. http://dx.doi.org/10.1016/j.ccr.2023.215192.
Texto completo da fonteNagel, Ulrich, e Christoph Roller. "Enantioselektive Katalyse, XVIII Der Einfluß nicht koordinierter Stereozentren auf die enantioselektive Hydrierung/Enantioselective Catalysis, XVIII The Influence of Non-Coordinated Stereocenters on the Enantioselective Hydrogenation". Zeitschrift für Naturforschung B 53, n.º 2 (1 de fevereiro de 1998): 211–23. http://dx.doi.org/10.1515/znb-1998-0213.
Texto completo da fonteGrabulosa, Arnald, Alberto Mannu, Guillermo Muller, Teresa Calvet e Mercè Font-Bardia. "P-Stereogenic monophosphines in Pd-catalysed enantioselective hydrovinylation of styrene". Journal of Organometallic Chemistry 696, n.º 11-12 (junho de 2011): 2338–45. http://dx.doi.org/10.1016/j.jorganchem.2011.02.034.
Texto completo da fonteRamazanova, Kyzgaldak, Soumyadeep Chakrabortty, Bernd H. Müller, Peter Lönnecke, Johannes G. de Vries e Evamarie Hey-Hawkins. "Synthesis of P-stereogenic 1-phosphanorbornane-derived phosphine–phosphite ligands and application in asymmetric catalysis". RSC Advances 13, n.º 49 (2023): 34439–44. http://dx.doi.org/10.1039/d3ra07630j.
Texto completo da fonteÁlvarez-Yebra, Rubén, Pep Rojo, Antoni Riera e Xavier Verdaguer. "Iridium complexes with P-stereogenic phosphino imidazole ligands: Synthesis, structure and catalysis". Tetrahedron 75, n.º 32 (agosto de 2019): 4358–64. http://dx.doi.org/10.1016/j.tet.2019.04.032.
Texto completo da fonteZhang, Jieming, Hang Ni, Qi Wu, Junfeng Yang e Junliang Zhang. "Development of P, S and Si-Stereogenic Compounds Synthesis via Palladium Catalysis". Chinese Journal of Organic Chemistry 42, n.º 10 (2022): 3118. http://dx.doi.org/10.6023/cjoc202208043.
Texto completo da fonteSondenecker, Aline, Ján Cvengroš, Raphael Aardoom e Antonio Togni. "P-Stereogenic Ferrocene-Based (Trifluoromethyl)phosphanes: Synthesis, Structure, Coordination Properties and Catalysis". European Journal of Organic Chemistry 2011, n.º 1 (12 de novembro de 2010): 78–87. http://dx.doi.org/10.1002/ejoc.201001162.
Texto completo da fonteHan, Zhengxu S., Li Zhang, Yibo Xu, Joshua D. Sieber, Maurice A. Marsini, Zhibin Li, Jonathan T. Reeves et al. "Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design". Angewandte Chemie International Edition 54, n.º 18 (10 de março de 2015): 5474–77. http://dx.doi.org/10.1002/anie.201500350.
Texto completo da fonteHan, Zhengxu S., Li Zhang, Yibo Xu, Joshua D. Sieber, Maurice A. Marsini, Zhibin Li, Jonathan T. Reeves et al. "Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design". Angewandte Chemie 127, n.º 18 (10 de março de 2015): 5564–67. http://dx.doi.org/10.1002/ange.201500350.
Texto completo da fonteBerger, Olivier, e Jean-Luc Montchamp. "A General Strategy for the Synthesis of P-Stereogenic Compounds". Angewandte Chemie International Edition 52, n.º 43 (9 de setembro de 2013): 11377–80. http://dx.doi.org/10.1002/anie.201306628.
Texto completo da fonteBalkaner, Orçun, Derya Işıl Sarıoğulları e Aylin Uslu. "A synthetic strategy of P-stereogenic ligands for catalysis: Examples based on cyclotriphosphazenes". Journal of Molecular Structure 1261 (agosto de 2022): 132834. http://dx.doi.org/10.1016/j.molstruc.2022.132834.
Texto completo da fonteCabré, Albert, Antoni Riera e Xavier Verdaguer. "P-Stereogenic Amino-Phosphines as Chiral Ligands: From Privileged Intermediates to Asymmetric Catalysis". Accounts of Chemical Research 53, n.º 3 (27 de fevereiro de 2020): 676–89. http://dx.doi.org/10.1021/acs.accounts.9b00633.
Texto completo da fonteHarvey, James Stephen, e Véronique Gouverneur. "Catalytic enantioselective synthesis of P-stereogenic compounds". Chemical Communications 46, n.º 40 (2010): 7477. http://dx.doi.org/10.1039/c0cc01939a.
Texto completo da fonteDziuba, Kamil, Małgorzata Lubańska e K. Michał Pietrusiewicz. "Enantiodivergent Synthesis of Both PAMPO Enantiomers Using l-Menthyl Chloroacetate and Stereomutation at P in Classical Quaternisation Reactions". Synthesis 52, n.º 06 (4 de dezembro de 2019): 909–16. http://dx.doi.org/10.1055/s-0039-1691531.
Texto completo da fonteVinokurov, Nikolai, K. Michał Pietrusiewicz, Sławomir Frynas, Michael Wiebcke e Holger Butenschön. "Asymmetric 1,3-dipolar cycloaddition with a P-stereogenic dipolarophile: An efficient approach to novel P-stereogenic 1,2-diphosphine systems". Chemical Communications, n.º 42 (2008): 5408. http://dx.doi.org/10.1039/b810573a.
Texto completo da fonteWhittaker, Benjamin, Manuel de Lera Ruiz e Christopher J. Hayes. "Stereoselective synthesis of highly functionalised P-stereogenic nucleosides via palladium-catalysed P–C cross-coupling reactions". Tetrahedron Letters 49, n.º 49 (dezembro de 2008): 6984–87. http://dx.doi.org/10.1016/j.tetlet.2008.09.102.
Texto completo da fonteBuergler, Jonas F., Katrin Niedermann e Antonio Togni. "P-Stereogenic Trifluoromethyl Derivatives of Josiphos: Synthesis, Coordination Properties, and Applications in Asymmetric Catalysis". Chemistry - A European Journal 18, n.º 2 (8 de dezembro de 2011): 632–40. http://dx.doi.org/10.1002/chem.201102390.
Texto completo da fonteSchmitz, Christian, Walter Leitner e Giancarlo Franciò. "Synthesis of P-Stereogenic Phosphoramidite and Phosphorodiamidite Ligands and Their Application in Asymmetric Catalysis". European Journal of Organic Chemistry 2015, n.º 28 (12 de agosto de 2015): 6205–30. http://dx.doi.org/10.1002/ejoc.201500767.
Texto completo da fonteHan, Zhengxu S., e et al. "ChemInform Abstract: Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design." ChemInform 46, n.º 36 (20 de agosto de 2015): no. http://dx.doi.org/10.1002/chin.201536217.
Texto completo da fonteMutlu, Ömer Faruk, Arzu Binici, Aytuğ Okumuş, Gamze Elmas, Bünyemin Çoşut, Zeynel Kılıç e Tuncer Hökelek. "Phosphorus–nitrogen compounds. Part 54. syntheses of chiral amino-4-fluorobenzyl-spiro(N/O)cyclotriphosphazenes: structural and stereogenic properties". New Journal of Chemistry 45, n.º 27 (2021): 12178–92. http://dx.doi.org/10.1039/d1nj00934f.
Texto completo da fonteImoto, Hiroaki, Yasuhiro Morisaki e Yoshiki Chujo. "Synthesis and coordination behaviors of P-stereogenic polymers". Chemical Communications 46, n.º 40 (2010): 7542. http://dx.doi.org/10.1039/c0cc03120h.
Texto completo da fonteDorta, Romano, Alberto Herrera, Anthony Linden, Frank Heinemann, René-Chris Brachvogel e Max von Delius. "Optimized Syntheses of Optically Pure P-Alkene Ligands: Crystal Structures of a Pair of P-Stereogenic Diastereomers". Synthesis 48, n.º 08 (17 de fevereiro de 2016): 1117–21. http://dx.doi.org/10.1055/s-0035-1560410.
Texto completo da fonteJoin, Benoît, David Mimeau, Olivier Delacroix e Annie-Claude Gaumont. "Pallado-catalysed hydrophosphination of alkynes: access to enantio-enriched P-stereogenic vinyl phosphine–boranes". Chem. Commun., n.º 30 (2006): 3249–51. http://dx.doi.org/10.1039/b607434k.
Texto completo da fonteChrist, M. Lorraine, Maria Zablocka, Sally Spencer, Rebecca J. Lavender, Marc Lemaire e Jean Pierre Majoral. "Cyclic β-iminophosphine: New P-stereogenic ligand for the asymmetric catalysed hydrogenation of ketones". Journal of Molecular Catalysis A: Chemical 245, n.º 1-2 (fevereiro de 2006): 210–16. http://dx.doi.org/10.1016/j.molcata.2005.09.043.
Texto completo da fonteClavero, Pau, Arnald Grabulosa, Mercè Font-Bardia e Guillermo Muller. "P-Stereogenic monophosphines with the 2-p-terphenylyl and 1-pyrenyl substituents. Application to Pd and Ru asymmetric catalysis". Journal of Molecular Catalysis A: Chemical 391 (setembro de 2014): 183–90. http://dx.doi.org/10.1016/j.molcata.2014.04.026.
Texto completo da fonteSchmitz, Christian, Walter Leitner e Giancarlo Francio. "ChemInform Abstract: Synthesis of P-Stereogenic Phosphoramidite and Phosphorodiamidite Ligands and Their Application in Asymmetric Catalysis." ChemInform 47, n.º 7 (janeiro de 2016): no. http://dx.doi.org/10.1002/chin.201607021.
Texto completo da fonteClarke, Eoin F., Eoin Rafter, Helge Müller-Bunz, Lee J. Higham e Declan G. Gilheany. "The synthesis of P-stereogenic MOP analogues and their use in rhodium catalysed asymmetric addition". Journal of Organometallic Chemistry 696, n.º 23 (novembro de 2011): 3608–15. http://dx.doi.org/10.1016/j.jorganchem.2011.08.010.
Texto completo da fonteNishida, Goushi, Keiichi Noguchi, Masao Hirano e Ken Tanaka. "Enantioselective Synthesis of P-Stereogenic Alkynylphosphine Oxides by Rh-Catalyzed [2+2+2] Cycloaddition". Angewandte Chemie International Edition 47, n.º 18 (21 de abril de 2008): 3410–13. http://dx.doi.org/10.1002/anie.200800144.
Texto completo da fonteVinokurov, Nikolai, K. Michal Pietrusiewicz e Holger Butenschön. "Asymmetric Diels–Alder cycloaddition of a di-P-stereogenic dienophile with cyclopentadiene". Tetrahedron: Asymmetry 20, n.º 9 (maio de 2009): 1081–85. http://dx.doi.org/10.1016/j.tetasy.2009.03.022.
Texto completo da fonteReichl, Kyle D., Daniel H. Ess e Alexander T. Radosevich. "Catalyzing Pyramidal Inversion: Configurational Lability of P-Stereogenic Phosphines via Single Electron Oxidation". Journal of the American Chemical Society 135, n.º 25 (17 de junho de 2013): 9354–57. http://dx.doi.org/10.1021/ja404943x.
Texto completo da fonteBergin, Enda, Cormac T. O'Connor, Shane B. Robinson, Eoghan M. McGarrigle, Colm P. O'Mahony e Declan G. Gilheany. "Synthesis of P-Stereogenic Phosphorus Compounds. Asymmetric Oxidation of Phosphines under Appel Conditions". Journal of the American Chemical Society 129, n.º 31 (agosto de 2007): 9566–67. http://dx.doi.org/10.1021/ja072925l.
Texto completo da fonteHuang, Zhijian, Xuan Huang, Baosheng Li, Chengli Mou, Song Yang, Bao-An Song e Yonggui Robin Chi. "Access to P-Stereogenic Phosphinates via N-Heterocyclic Carbene-Catalyzed Desymmetrization of Bisphenols". Journal of the American Chemical Society 138, n.º 24 (10 de junho de 2016): 7524–27. http://dx.doi.org/10.1021/jacs.6b04624.
Texto completo da fonteScriban, Corina, e David S. Glueck. "Platinum-Catalyzed Asymmetric Alkylation of Secondary Phosphines: Enantioselective Synthesis of P-Stereogenic Phosphines". Journal of the American Chemical Society 128, n.º 9 (março de 2006): 2788–89. http://dx.doi.org/10.1021/ja058096q.
Texto completo da fonteHarvey, James Stephen, Steven J Malcolmson, Katherine S Dunne, Simon J Meek, Amber L Thompson, Richard R Schrock, Amir H Hoveyda e Véronique Gouverneur. "Enantioselective Synthesis of P-Stereogenic Phosphinates and Phosphine Oxides by Molybdenum-Catalyzed Asymmetric Ring-Closing Metathesis". Angewandte Chemie International Edition 48, n.º 4 (12 de janeiro de 2009): 762–66. http://dx.doi.org/10.1002/anie.200805066.
Texto completo da fonteGranander, Johan, Francesco Secci, Peter O’Brien e Brian Kelly. "Kinetic resolution of P-stereogenic phosphine boranes via deprotonation using s-butyllithium/(−)-sparteine". Tetrahedron: Asymmetry 20, n.º 21 (novembro de 2009): 2432–34. http://dx.doi.org/10.1016/j.tetasy.2009.10.026.
Texto completo da fonteMoulin, Dominique, Sébastien Bago, Christophe Bauduin, Christophe Darcel e Sylvain Jugé. "Asymmetric synthesis of P-stereogenic o-hydroxyaryl-phosphine (borane) and phosphine-phosphinite ligands". Tetrahedron: Asymmetry 11, n.º 19 (outubro de 2000): 3939–56. http://dx.doi.org/10.1016/s0957-4166(00)00372-4.
Texto completo da fonteWilliams, B. Scott, Paulo Dani, Martin Lutz, Anthony L Spek e Gerard van Koten. "Development of the First P-Stereogenic PCP Pincer Ligands, Their Metallation by Palladium and Platinum, and Preliminary Catalysis". Helvetica Chimica Acta 84, n.º 11 (14 de novembro de 2001): 3519–30. http://dx.doi.org/10.1002/1522-2675(20011114)84:11<3519::aid-hlca3519>3.0.co;2-9.
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