Artigos de revistas sobre o tema "Salen chiraux"
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Gualandi, Andrea, Francesco Calogero, Simone Potenti e Pier Giorgio Cozzi. "Al(Salen) Metal Complexes in Stereoselective Catalysis". Molecules 24, n.º 9 (2 de maio de 2019): 1716. http://dx.doi.org/10.3390/molecules24091716.
Texto completo da fonteAdão, Pedro, Mannar R. Maurya, Umesh Kumar, Fernando Avecilla, Rui T. Henriques, Maxim L. Kusnetsov, João Costa Pessoa e Isabel Correia. "Vanadium-salen and -salan complexes: Characterization and application in oxygen-transfer reactions". Pure and Applied Chemistry 81, n.º 7 (30 de junho de 2009): 1279–96. http://dx.doi.org/10.1351/pac-con-08-09-07.
Texto completo da fonteZuo, Shengli, Shuxiang Zheng, Jianjun Liu e Ang Zuo. "Mechanochemical synthesis of unsymmetrical salens for the preparation of Co–salen complexes and their evaluation as catalysts for the synthesis of α-aryloxy alcohols via asymmetric phenolic kinetic resolution of terminal epoxides". Beilstein Journal of Organic Chemistry 18 (10 de outubro de 2022): 1416–23. http://dx.doi.org/10.3762/bjoc.18.147.
Texto completo da fonteKarukurichi, Kannan R., Xiang Fei, Robert A. Swyka, Sylvain Broussy, Weijun Shen, Sangeeta Dey, Sandip K. Roy e David B. Berkowitz. "Mini-ISES identifies promising carbafructopyranose-based salens for asymmetric catalysis: Tuning ligand shape via the anomeric effect". Science Advances 1, n.º 6 (julho de 2015): e1500066. http://dx.doi.org/10.1126/sciadv.1500066.
Texto completo da fonteChaudhary, Pooja, Geeta Devi Yadav, Krishna K. Damodaran e Surendra Singh. "Synthesis of new chiral Mn(iii)–salen complexes as recoverable and reusable homogeneous catalysts for the asymmetric epoxidation of styrenes and chromenes". New Journal of Chemistry 46, n.º 3 (2022): 1308–18. http://dx.doi.org/10.1039/d1nj04758b.
Texto completo da fonteSoundararajan, Karthikeyan, Helen Ratna Monica Jeyarajan, Raju Subimol Kamarajapurathu e Karthik Krishna Kumar Ayyanoth. "Facile and innovative catalytic protocol for intramolecular Friedel–Crafts cyclization of Morita–Baylis–Hillman adducts: Synergistic combination of chiral (salen)chromium(III)/BF3·OEt2 catalysis". Beilstein Journal of Organic Chemistry 17 (26 de agosto de 2021): 2186–93. http://dx.doi.org/10.3762/bjoc.17.140.
Texto completo da fonteIkbal, Sk Asif, Yoko Sakata e Shigehisa Akine. "A chiral spirobifluorene-based bis(salen) zinc(ii) receptor towards highly enantioselective binding of chiral carboxylates". Dalton Transactions 50, n.º 12 (2021): 4119–23. http://dx.doi.org/10.1039/d1dt00218j.
Texto completo da fonteJia, Yihong, Asma A. Alothman, Rui Liang, Xiaoyong Li, Weiyi Ouyang, Xiangdong Wang, Yong Wu et al. "Oligomeric (Salen)Mn(III) Complexes Featuring Tartrate Linkers Immobilized over Layered Double Hydroxide for Catalytically Asymmetric Epoxidation of Unfunctionalized Olefins". Materials 13, n.º 21 (29 de outubro de 2020): 4860. http://dx.doi.org/10.3390/ma13214860.
Texto completo da fontePappalardo, Andrea, Francesco P. Ballistreri, Rosa Maria Toscano, Maria Assunta Chiacchio, Laura Legnani, Giovanni Grazioso, Lucia Veltri e Giuseppe Trusso Sfrazzetto. "Alkene Epoxidations Mediated by Mn-Salen Macrocyclic Catalysts". Catalysts 11, n.º 4 (2 de abril de 2021): 465. http://dx.doi.org/10.3390/catal11040465.
Texto completo da fonteKim, Sung Soo. "Asymmetric cyanohydrin synthesis from aldehydes and ketones using chiral metal (salen) complex as catalyst". Pure and Applied Chemistry 78, n.º 5 (1 de janeiro de 2006): 977–83. http://dx.doi.org/10.1351/pac200678050977.
Texto completo da fonteSaravanan, S., Noor-ul H. Khan, Ajay Jakhar, Amamudin Ansari, Rukhsana I. Kureshy, Sayed H. R. Abdi e Gaurav Kumar. "Enantioselective Strecker reaction of aldimines using potassium cyanide catalyzed by a recyclable macrocyclic V(v) salen complex". RSC Advances 5, n.º 121 (2015): 99951–58. http://dx.doi.org/10.1039/c5ra18914d.
Texto completo da fonteTanaka, Daiki, Wataru Kawakubo, Erika Tsuda, Yuya Mitsumoto, Dong Hyun Yoon, Tetsushi Sekiguchi, Takashiro Akitsu e Shuichi Shoji. "Microfluidic synthesis of chiral salen Mn(ii) and Co(ii) complexes containing lysozyme". RSC Advances 6, n.º 85 (2016): 81862–68. http://dx.doi.org/10.1039/c6ra09975k.
Texto completo da fonteRoy, Tamal, Sunirmal Barik, Manish Kumar, Rukhsana I. Kureshy, Bishwajit Ganguly, Noor-ul H. Khan, Sayed H. R. Abdi e Hari C. Bajaj. "Asymmetric hydrolytic kinetic resolution with recyclable polymeric Co(iii)–salen complexes: a practical strategy in the preparation of (S)-metoprolol, (S)-toliprolol and (S)-alprenolol: computational rationale for enantioselectivity". Catal. Sci. Technol. 4, n.º 11 (2014): 3899–908. http://dx.doi.org/10.1039/c4cy00594e.
Texto completo da fonteGao, Bo, Dongni Li, Yanhui Li, Qian Duan, Ranlong Duan e Xuan Pang. "Ring-opening polymerization of lactide using chiral salen aluminum complexes as initiators: high productivity and stereoselectivity". New Journal of Chemistry 39, n.º 6 (2015): 4670–75. http://dx.doi.org/10.1039/c5nj00469a.
Texto completo da fontePuglisi, Roberta, Francesco P. Ballistreri, Chiara M. A. Gangemi, Rosa Maria Toscano, Gaetano A. Tomaselli, Andrea Pappalardo e Giuseppe Trusso Sfrazzetto. "Chiral Zn–salen complexes: a new class of fluorescent receptors for enantiodiscrimination of chiral amines". New Journal of Chemistry 41, n.º 3 (2017): 911–15. http://dx.doi.org/10.1039/c6nj03592b.
Texto completo da fonteXi, Xiuxing, Jing Shao, Xingbang Hu e Youting Wu. "Structure and asymmetric epoxidation reactivity of chiral Mn(iii) salen catalysts modified by different axial anions". RSC Advances 5, n.º 98 (2015): 80772–78. http://dx.doi.org/10.1039/c5ra13178b.
Texto completo da fonteLi, Jiawei, Yanwei Ren, Chaorong Qi e Huanfeng Jiang. "The first porphyrin–salen based chiral metal–organic framework for asymmetric cyanosilylation of aldehydes". Chemical Communications 53, n.º 58 (2017): 8223–26. http://dx.doi.org/10.1039/c7cc03499g.
Texto completo da fonteSong, Feijie, Teng Zhang, Cheng Wang e Wenbin Lin. "Chiral porous metal-organic frameworks with dual active sites for sequential asymmetric catalysis". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 468, n.º 2143 (14 de março de 2012): 2035–52. http://dx.doi.org/10.1098/rspa.2012.0100.
Texto completo da fonteQu, Lang, Chunbo Li, Guangyu Shen, Fei Gou, Jintong Song, Man Wang, Xuemei Xu, Xiangge Zhou e Haifeng Xiang. "Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands". Materials Chemistry Frontiers 3, n.º 6 (2019): 1199–208. http://dx.doi.org/10.1039/c9qm00105k.
Texto completo da fonteLee, Kwang Yeon, Young Hee Lee, Chang Kyo Shin e Geon Joong Kim. "Chiral (Salen) Complexes Encapsulated in Mesoporous ZSM-5 as an Optical Active Catalyst for Asymmetric Phenolic Ring Opening of Terminal Epoxides". Solid State Phenomena 124-126 (junho de 2007): 1809–12. http://dx.doi.org/10.4028/www.scientific.net/ssp.124-126.1809.
Texto completo da fonteGao, Mengqiao, Rong Tan, Pengbo Hao, Yaoyao Zhang, Jiang Deng e Donghong Yin. "Ultraviolet-responsive self-assembled metallomicelles for photocontrollable catalysis of asymmetric sulfoxidation in water". RSC Advances 7, n.º 86 (2017): 54570–80. http://dx.doi.org/10.1039/c7ra11022g.
Texto completo da fonteXing, Chen, Jiang Deng, Rong Tan, Mengqiao Gao, Pengbo Hao, Donghong Yin e Dulin Yin. "Cooperative chiral salen TiIV catalyst supported on ionic liquid-functionalized graphene oxide accelerates asymmetric sulfoxidation in water". Catalysis Science & Technology 7, n.º 24 (2017): 5944–52. http://dx.doi.org/10.1039/c7cy01511a.
Texto completo da fonteWang, Weiying, Chaoping Li, Yibing Pi, Jiajun Wang, Rong Tan e Donghong Yin. "Chiral salen Cr(iii) complexes encapsulated in thermo-responsive polymer nanoreactors for asymmetric epoxidation of alkenes in water". Catalysis Science & Technology 9, n.º 20 (2019): 5626–35. http://dx.doi.org/10.1039/c9cy01398a.
Texto completo da fonteSavchuk, Mariia, Steven Vertueux, Thomas Cauchy, Matthieu Loumaigne, Francesco Zinna, Lorenzo Di Bari, Nicolas Zigon e Narcis Avarvari. "Schiff-base [4]helicene Zn(ii) complexes as chiral emitters". Dalton Transactions 50, n.º 30 (2021): 10533–39. http://dx.doi.org/10.1039/d1dt01752g.
Texto completo da fonteShen, Guangyu, Fei Gou, Jinghui Cheng, Xiaohong Zhang, Xiangge Zhou e Haifeng Xiang. "Chiral and non-conjugated fluorescent salen ligands: AIE, anion probes, chiral recognition of unprotected amino acids, and cell imaging applications". RSC Advances 7, n.º 64 (2017): 40640–49. http://dx.doi.org/10.1039/c7ra08267c.
Texto completo da fonteBandini, Marco, Pier Giorgio Cozzi e Achille Umani-Ronchi. "Asymmetric synthesis with "privileged" ligands". Pure and Applied Chemistry 73, n.º 2 (1 de janeiro de 2001): 325–29. http://dx.doi.org/10.1351/pac200173020325.
Texto completo da fonteHuang, J., D. W. Qi, J. L. Cai e X. H. Chen. "Retraction: Olefin epoxidation with chiral salen Mn(iii) immobilized on ZnPS-PVPA upon alkyldiamine". RSC Advances 10, n.º 70 (2020): 43010. http://dx.doi.org/10.1039/d0ra90126a.
Texto completo da fonteZabierowski, Piotr, Janusz Szklarzewicz, Ryszard Gryboś, Barbara Modryl e Wojciech Nitek. "Assemblies of salen-type oxidovanadium(iv) complexes: substituent effects and in vitro protein tyrosine phosphatase inhibition". Dalton Trans. 43, n.º 45 (2014): 17044–53. http://dx.doi.org/10.1039/c4dt02344g.
Texto completo da fonteFu, Wenqin, Yibing Pi, Mengqiao Gao, Weiying Wang, Chaoping Li, Rong Tan e Donghong Yin. "Light-controlled cooperative catalysis of asymmetric sulfoxidation based on azobenzene-bridged chiral salen TiIV catalysts". Chemical Communications 56, n.º 44 (2020): 5993–96. http://dx.doi.org/10.1039/c9cc09827e.
Texto completo da fonteChen, Danping, Ran Luo, Meiyan Li, Mengqi Wen, Yan Li, Chao Chen e Ning Zhang. "Salen(Co(iii)) imprisoned within pores of a metal–organic framework by post-synthetic modification and its asymmetric catalysis for CO2 fixation at room temperature". Chemical Communications 53, n.º 79 (2017): 10930–33. http://dx.doi.org/10.1039/c7cc06522a.
Texto completo da fonteRoy, Susmita, Piyali Bhanja, Sk Safikul Islam, Asim Bhaumik e Sk Manirul Islam. "A new chiral Fe(iii)–salen grafted mesoporous catalyst for enantioselective asymmetric ring opening of racemic epoxides at room temperature under solvent-free conditions". Chemical Communications 52, n.º 9 (2016): 1871–74. http://dx.doi.org/10.1039/c5cc08675b.
Texto completo da fonteZheng, Weiguo, Rong Tan, Shenfu Yin, Yaoyao Zhang, Guangwu Zhao, Yaju Chen e Donghong Yin. "Ionic liquid-functionalized graphene oxide as an efficient support for the chiral salen Mn(iii) complex in asymmetric epoxidation of unfunctionalized olefins". Catalysis Science & Technology 5, n.º 4 (2015): 2092–102. http://dx.doi.org/10.1039/c4cy01290a.
Texto completo da fonteXia, Xuexiu, Chengrong Lu, Bei Zhao e Yingming Yao. "Lanthanide complexes combined with chiral salen ligands: application in the enantioselective epoxidation reaction of α,β-unsaturated ketones". RSC Advances 9, n.º 24 (2019): 13749–56. http://dx.doi.org/10.1039/c9ra01529a.
Texto completo da fonteZhang, Yaoyao, Rong Tan, Mengqiao Gao, Pengbo Hao e Donghong Yin. "Bio-inspired single-chain polymeric nanoparticles containing a chiral salen TiIV complex for highly enantioselective sulfoxidation in water". Green Chemistry 19, n.º 4 (2017): 1182–93. http://dx.doi.org/10.1039/c6gc02743a.
Texto completo da fonteIslam, Md Mominul, Piyali Bhanja, Mita Halder, Sudipta K. Kundu, Asim Bhaumik e Sk Manirul Islam. "Chiral Co(iii)–salen complex supported over highly ordered functionalized mesoporous silica for enantioselective aminolysis of racemic epoxides". RSC Advances 6, n.º 111 (2016): 109315–21. http://dx.doi.org/10.1039/c6ra21523h.
Texto completo da fonteZhang, Yaoyao, Rong Tan, Mengqiao Gao, Pengbo Hao e Donghong Yin. "Correction: Bio-inspired single-chain polymeric nanoparticles containing a chiral salen TiIV complex for highly enantioselective sulfoxidation in water". Green Chemistry 19, n.º 4 (2017): 1194. http://dx.doi.org/10.1039/c7gc90011b.
Texto completo da fonteBhunia, Asamanjoy, Subarna Dey, José María Moreno, Urbano Diaz, Patricia Concepcion, Kristof Van Hecke, Christoph Janiak e Pascal Van Der Voort. "A homochiral vanadium–salen based cadmium bpdc MOF with permanent porosity as an asymmetric catalyst in solvent-free cyanosilylation". Chemical Communications 52, n.º 7 (2016): 1401–4. http://dx.doi.org/10.1039/c5cc09459c.
Texto completo da fonteHuang, Jing, Xiangkai Fu, Gang Wang, Qiang Miao e Guomin Wang. "Correction: Axially coordinated chiral salen Mn(iii) anchored onto azole onium modified ZnPS-PVPA as effective catalysts for asymmetric epoxidation of unfunctionalized olefins". Dalton Transactions 50, n.º 23 (2021): 8258. http://dx.doi.org/10.1039/d1dt90084f.
Texto completo da fonteD'Urso, Alessandro, Cristina Tudisco, Francesco P. Ballistreri, Guglielmo G. Condorelli, Rosalba Randazzo, Gaetano A. Tomaselli, Rosa M. Toscano, Giuseppe Trusso Sfrazzetto e Andrea Pappalardo. "Enantioselective extraction mediated by a chiral cavitand–salen covalently assembled on a porous silicon surface". Chem. Commun. 50, n.º 39 (2014): 4993–96. http://dx.doi.org/10.1039/c4cc00034j.
Texto completo da fonteZhao, Changjia, e Mukund Sibi. "Enantioselective and Diastereoselective Conjugate Radical Additions to α-Arylidene Ketones and Lactones". Synlett 28, n.º 20 (20 de outubro de 2017): 2971–75. http://dx.doi.org/10.1055/s-0036-1590930.
Texto completo da fonteZhang, Yaoyao, Rong Tan, Guangwu Zhao, Xuanfeng Luo e Donghong Yin. "Asymmetric epoxidation of unfunctionalized olefins accelerated by thermoresponsive self-assemblies in aqueous systems". Catalysis Science & Technology 6, n.º 2 (2016): 488–96. http://dx.doi.org/10.1039/c5cy00953g.
Texto completo da fonteZhang, Mingjie, Zhiyang Tang, Wenqin Fu, Weiying Wang, Rong Tan e Donghong Yin. "An ionic liquid-functionalized amphiphilic Janus material as a Pickering interfacial catalyst for asymmetric sulfoxidation in water". Chemical Communications 55, n.º 5 (2019): 592–95. http://dx.doi.org/10.1039/c8cc08292h.
Texto completo da fonteLi, Jiawei, Yanwei Ren, Chaorong Qi e Huanfeng Jiang. "A chiral salen-based MOF catalytic material with high thermal, aqueous and chemical stabilities". Dalton Transactions 46, n.º 24 (2017): 7821–32. http://dx.doi.org/10.1039/c7dt01116d.
Texto completo da fonteZhao, Guangwu, Rong Tan, Yaoyao Zhang, Xuanfeng Luo, Chen Xing e Donghong Yin. "Cooperative chiral salen TiIV catalysts with built-in phase-transfer capability accelerate asymmetric sulfoxidation in water". RSC Advances 6, n.º 29 (2016): 24704–11. http://dx.doi.org/10.1039/c6ra01130f.
Texto completo da fonteHuang, Jing, Xiangkai Fu, Gang Wang, Yaqin Ge e Qiang Miao. "Retraction: A series of novel types of immobilized chiral salen Mn(iii) on different organic polymer–inorganic hybrid crystalline zinc phosphonate–phosphate act as catalysts for asymmetric epoxidation of unfunctionalized olefins". Catalysis Science & Technology 11, n.º 11 (2021): 3932. http://dx.doi.org/10.1039/d1cy90049h.
Texto completo da fonteHuang, Jing, Xiangkai Fu e Qiang Miao. "Retraction: Synthesis of a novel type of chiral salen Mn(iii) complex immobilized on crystalline zinc poly(styrene-phenylvinylphosphonate)-phosphate (ZnPS-PVPP) as effective catalysts for asymmetric epoxidation of unfunctionalized olefins". Catalysis Science & Technology 11, n.º 11 (2021): 3931. http://dx.doi.org/10.1039/d1cy90048j.
Texto completo da fonteZhou, Xiangge, Jin Zhao, Ana M. Santos e Fritz E. Kühn. "Molybdenum(VI) cis-Dioxo Complexes with Chiral Schiff Base Ligands: Synthesis, Characterization, and Catalytic Applications". Zeitschrift für Naturforschung B 59, n.º 11-12 (1 de dezembro de 2004): 1223–28. http://dx.doi.org/10.1515/znb-2004-11-1240.
Texto completo da fonteSunaga, Nobumitsu, Tomoyuki Haraguchi e Takashiro Akitsu. "Orientation of Chiral Schiff Base Metal Complexes Involving Azo-Groups for Induced CD on Gold Nanoparticles by Polarized UV Light Irradiation". Symmetry 11, n.º 9 (2 de setembro de 2019): 1094. http://dx.doi.org/10.3390/sym11091094.
Texto completo da fonteZou, Xiaochuan, Yue Wang, Cun Wang, Kaiyun Shi, Yanrong Ren e Xin Zhao. "Chiral MnIII (Salen) Immobilized on Organic Polymer/Inorganic Zirconium Hydrogen Phosphate Functionalized with 3-Aminopropyltrimethoxysilane as an Efficient and Recyclable Catalyst for Enantioselective Epoxidation of Styrene". Polymers 11, n.º 2 (26 de janeiro de 2019): 212. http://dx.doi.org/10.3390/polym11020212.
Texto completo da fonteDu, Xia, Zijian Li, Yan Liu, Shiping Yang e Yong Cui. "Chiral porous metal–organic frameworks containing μ-oxo-bis[Ti(salan)] units for asymmetric cyanation of aldehydes". Dalton Transactions 44, n.º 29 (2015): 12999–3002. http://dx.doi.org/10.1039/c5dt01682g.
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