Trisoxazoliny (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Trisoxazoliny" in Czech language version.

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14doi.org

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10nih.gov

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1harvard.edu

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doi.org

Benjamin D. Ward; Lutz H. Gade. Rare earth metal oxazoline complexes in asymmetric catalysis. Chemical Communications. 2012, s. 10587–10599. doi:10.1039/c2cc34997c. PMID 22982883.
Jian Zhou; Yong Tang. The development and application of chiral trisoxazolines in asymmetric catalysis and molecular recognition. Chemical Society Reviews. 2005, s. 664–676. doi:10.1039/c2cc34997c. PMID 16186896.
Lutz H. Gade, Guido Marconi, Clémence Dro, Benjamin D. Ward, Macarena Poyatos, Stéphane Bellemin-Laponnaz, Hubert Wadepohl, Lorenzo Sorace, Giordano Poneti. Shaping and Enforcing Coordination Spheres: The Implications of C3 and C1 Chirality in the Coordination Chemistry of 1,1,1-Tris(oxazolinyl)ethane ("Trisox"). Chemistry: A European Journal. 2007, s. 3058–3075. doi:10.1002/chem.200601651. PMID 17300108.
Lutz H. Gade; Stéphane Bellemin-Laponnaz. Exploiting Threefold Symmetry in Asymmetric Catalysis: The Case of Tris(oxazolinyl)ethanes ("Trisox"). Chemistry: A European Journal. 2008, s. 4142–4152. doi:10.1002/chem.200701990. PMID 18348150.
Carole Foltz; Björn Stecker; Guido Marconi; Stéphane Bellemin-Laponnaz; Hubert Wadepohl; Lutz H. Gade. Stereochemical Consequences of Threefold Symmetry in Asymmetric Catalysis: Distorting C3 Chiral 1,1,1-Tris(oxazolinyl)ethanes ("Trisox") in CuII Lewis Acid Catalysts. Chemistry: A European Journal. 2007, s. 9912–9923. doi:10.1002/chem.200701085. PMID 17955557.
Hae-Jo Kim; Yeon-Hwan Kim; Jong-In Hong. Sugar recognition by C3-symmetric oxazoline hosts. Tetrahedron Letters. 2001, s. 5049–5052. doi:10.1016/S0040-4039(01)00915-7.
Ken-ichi Kawasaki; Tsutomu Katsuki. Enantioselective allylic oxidation of cycloalkenes by using Cu(II)-tris(oxazoline) complex as a catalyst. Tetrahedron. 1997, s. 6337–6350. doi:10.1016/S0040-4020(97)00322-0.
Stéphane Bellemin-Laponnaz; Lutz H. Gade. A Modular Approach to C1 and C3 Chiral N-Tripodal Ligands for Asymmetric Catalysis. Angewandte Chemie International Edition. 2002, s. 3473–3475. doi:10.1002/1521-3773(20020916)41:18<3473::AID-ANIE3473>3.0.CO;2-N. PMID 12298069.
Meng-Chun Ye; Bin Li; Jian Zhou; Xiu-Li Sun; Yong Tang. Modular Synthesis of Chiral Homo- and Heterotrisoxazolines: Improving the Enantioselectivity in the Asymmetric Michael Addition of Indole to Benzylidene Malonate. The Journal of Organic Chemistry. 2005, s. 6108–6110. doi:10.1021/jo050595m. PMID 16018712.
Jian Zhou; Meng-Chun Ye; Zheng-Zheng Huang; Yong Tang. Controllable Enantioselective Friedel−Crafts Reaction between Indoles and Alkylidene Malonates Catalyzed by Pseudo-C₃-Symmetric Trisoxazoline Copper(II) Complexes. The Journal of Organic Chemistry. 2004, s. 1309–1320. doi:10.1021/jo035552p. PMID 14961685.
Giuseppe Zanoni; Francesca Castronovo; Maurizio Franzini; Yong TangGiovanni Vidari; Elios Giannini. Toggling enantioselective catalysis—a promising paradigm in the development of more efficient and versatile enantioselective synthetic methodologies. Chemical Society Reviews. 2003, s. 115–129. doi:10.1039/B201455F. PMID 12792935.
Lenka Lukešová; Benjamin D. Ward; Stéphane Bellemin-Laponnaz; Hubert Wadepohl; Lutz H. Gade. High tacticity control in organolanthanide polymerization catalysis: formation of isotactic poly(α-alkenes) with a chiral C3-symmetric thulium complex. Dalton Transactions. 2007, s. 920–922. doi:10.1039/B700269F. PMID 17308670.
Benjamin D. Ward; Lenka Lukešová; Hubert Wadepohl; Stéphane Bellemin-Laponnaz; Lutz H. Gade. Scandium-Catalyzed Polymerization of CH₃(CH₂)_nCH=CH₂ (n = 0–4): Remarkable Activity and Tacticity Control. European Journal of Inorganic Chemistry. 2009, s. 866–871. doi:10.1002/ejic.200801106.
Xiaohui Kang; Yuming Song; Yi Luo; Gang Li; Zhaomin Hou; Jingping Qu. Computational Studies on Isospecific Polymerization of 1-Hexene Catalyzed by Cationic Rare Earth Metal Alkyl Complex Bearing a Pr-trisox Ligand. Macromolecules. 2012, s. 640–651. doi:10.1021/ma202414k. Bibcode 2012MaMol..45..640K.

harvard.edu

adsabs.harvard.edu

Xiaohui Kang; Yuming Song; Yi Luo; Gang Li; Zhaomin Hou; Jingping Qu. Computational Studies on Isospecific Polymerization of 1-Hexene Catalyzed by Cationic Rare Earth Metal Alkyl Complex Bearing a Pr-trisox Ligand. Macromolecules. 2012, s. 640–651. doi:10.1021/ma202414k. Bibcode 2012MaMol..45..640K.

nih.gov

ncbi.nlm.nih.gov

Benjamin D. Ward; Lutz H. Gade. Rare earth metal oxazoline complexes in asymmetric catalysis. Chemical Communications. 2012, s. 10587–10599. doi:10.1039/c2cc34997c. PMID 22982883.
Jian Zhou; Yong Tang. The development and application of chiral trisoxazolines in asymmetric catalysis and molecular recognition. Chemical Society Reviews. 2005, s. 664–676. doi:10.1039/c2cc34997c. PMID 16186896.
Lutz H. Gade, Guido Marconi, Clémence Dro, Benjamin D. Ward, Macarena Poyatos, Stéphane Bellemin-Laponnaz, Hubert Wadepohl, Lorenzo Sorace, Giordano Poneti. Shaping and Enforcing Coordination Spheres: The Implications of C3 and C1 Chirality in the Coordination Chemistry of 1,1,1-Tris(oxazolinyl)ethane ("Trisox"). Chemistry: A European Journal. 2007, s. 3058–3075. doi:10.1002/chem.200601651. PMID 17300108.
Lutz H. Gade; Stéphane Bellemin-Laponnaz. Exploiting Threefold Symmetry in Asymmetric Catalysis: The Case of Tris(oxazolinyl)ethanes ("Trisox"). Chemistry: A European Journal. 2008, s. 4142–4152. doi:10.1002/chem.200701990. PMID 18348150.
Carole Foltz; Björn Stecker; Guido Marconi; Stéphane Bellemin-Laponnaz; Hubert Wadepohl; Lutz H. Gade. Stereochemical Consequences of Threefold Symmetry in Asymmetric Catalysis: Distorting C3 Chiral 1,1,1-Tris(oxazolinyl)ethanes ("Trisox") in CuII Lewis Acid Catalysts. Chemistry: A European Journal. 2007, s. 9912–9923. doi:10.1002/chem.200701085. PMID 17955557.
Stéphane Bellemin-Laponnaz; Lutz H. Gade. A Modular Approach to C1 and C3 Chiral N-Tripodal Ligands for Asymmetric Catalysis. Angewandte Chemie International Edition. 2002, s. 3473–3475. doi:10.1002/1521-3773(20020916)41:18<3473::AID-ANIE3473>3.0.CO;2-N. PMID 12298069.
Meng-Chun Ye; Bin Li; Jian Zhou; Xiu-Li Sun; Yong Tang. Modular Synthesis of Chiral Homo- and Heterotrisoxazolines: Improving the Enantioselectivity in the Asymmetric Michael Addition of Indole to Benzylidene Malonate. The Journal of Organic Chemistry. 2005, s. 6108–6110. doi:10.1021/jo050595m. PMID 16018712.
Jian Zhou; Meng-Chun Ye; Zheng-Zheng Huang; Yong Tang. Controllable Enantioselective Friedel−Crafts Reaction between Indoles and Alkylidene Malonates Catalyzed by Pseudo-C₃-Symmetric Trisoxazoline Copper(II) Complexes. The Journal of Organic Chemistry. 2004, s. 1309–1320. doi:10.1021/jo035552p. PMID 14961685.
Giuseppe Zanoni; Francesca Castronovo; Maurizio Franzini; Yong TangGiovanni Vidari; Elios Giannini. Toggling enantioselective catalysis—a promising paradigm in the development of more efficient and versatile enantioselective synthetic methodologies. Chemical Society Reviews. 2003, s. 115–129. doi:10.1039/B201455F. PMID 12792935.
Lenka Lukešová; Benjamin D. Ward; Stéphane Bellemin-Laponnaz; Hubert Wadepohl; Lutz H. Gade. High tacticity control in organolanthanide polymerization catalysis: formation of isotactic poly(α-alkenes) with a chiral C3-symmetric thulium complex. Dalton Transactions. 2007, s. 920–922. doi:10.1039/B700269F. PMID 17308670.