Polystyrene copolymer supported by substituted (1R,2R)-1, 2-diphenylethane-1,2-diamine-copper(II) complexes: a recyclable catalyst for asymmetric Henry reactions

被引:9
作者
Androvic, Ladislav [1 ]
Drabina, Pavel [1 ]
Panov, Illia [1 ]
Frumarova, Bozena [2 ]
Kalendova, Andrea [3 ]
Sedlak, Milos [1 ]
机构
[1] Univ Pardubice, Fac Chem Technol, Inst Organ Chem & Technol, Pardubice 53210, Czech Republic
[2] ASCR, Inst Macromol Chem, Prague 16206, Czech Republic
[3] Univ Pardubice, Fac Chem Technol, Inst Chem & Technol Macromol Mat, Pardubice 53210, Czech Republic
关键词
SUSPENSION POLYMERIZATION; COPPER(II) COMPLEXES; NITROALDOL REACTIONS; LIGANDS; RESINS; REAGENTS; BEADS;
D O I
10.1016/j.tetasy.2014.04.004
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein described the preparation of swelling pearl-like copolymer styrene-4-vinylbenzyl chloride crosslinked by means of tetra(ethylene glycol)-bis(4-vinylbenzyl)ether (200-800 mu m). The pearl-like polymer was used to anchor (1R,2R)-1-amino-2-(2,3-dihydro-1H-isoindole-2-yl)-1,2-diphenylethane by a covalent bond; the product was subsequently transformed into the corresponding complex with Cu(II) acetate. The synthesized catalyst was used for the catalysis of the Henry reaction of functionalized aldehydes with nitromethane in ethanol. The reactions proceeded in a polymeric matrix of the swelling catalyst at a rate comparable with the rates of reactions in a homogeneous medium. The corresponding functionalized 2-nitroethanols were formed in quantitative yields (20 degrees C, 24 h) with enantiomeric excess values of up to 96%. The catalyst was recycled five times without losing its effectiveness with regard to the yield and enantioselectivity; only a partial mechanical degradation of the polymeric matrix occurred due to stirring. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:775 / 780
页数:6
相关论文
共 34 条
[1]   The use of NIR-FT-Raman spectroscopy for the characterization of polymer-supported reagents and catalysts [J].
Altava, B ;
Burguete, MI ;
García-Verdugo, E ;
Luis, SV ;
Vicent, MJ .
TETRAHEDRON, 2001, 57 (41) :8675-8683
[2]  
Ananthi N, 2013, INDIAN J CHEM B, V 52, P87
[3]   Bis(oxazoline)-Based Coordination Polymers: A Recoverable System for Enantioselective Henry Reactions [J].
Angulo, Beatriz ;
Garcia, Jose I. ;
Herrerias, Clara I. ;
Mayoral, Jose A. ;
Minana, Ana C. .
JOURNAL OF ORGANIC CHEMISTRY, 2012, 77 (13) :5525-5532
[4]   Practical asymmetric henry reaction catalyzed by a chiral Diamine-Cu(OAc)2 complex [J].
Arai, Takayoshi ;
Watanabe, Masahiko ;
Yanagisawa, Akira .
ORGANIC LETTERS, 2007, 9 (18) :3595-3597
[5]   Formation of multi-stereogenic centers using a catalytic diastereoselective Henry reaction [J].
Arai, Takayoshi ;
Taneda, Yoshinori ;
Endo, Yoko .
CHEMICAL COMMUNICATIONS, 2010, 46 (42) :7936-7938
[6]  
ARAL T, 2006, ANGEW CHEM INT EDIT, V45, P5978
[7]   Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation [J].
Bandini, Marco ;
Benaglia, Maurizio ;
Sinisi, Riccardo ;
Tommasi, Simona ;
Umani-Ronchi, Achille .
ORGANIC LETTERS, 2007, 9 (11) :2151-2153
[8]   New highly asymmetric henry reaction catalyzed by CuII and a C1-Symmetric aminopyridine ligand, and its application to the synthesis of miconazole [J].
Blay, Gonzalo ;
Domingo, Luis R. ;
Hernandez-Olmos, Victor ;
Pedro, Jose R. .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (15) :4725-4730
[9]  
BNOSAIE DS, 2014, TETRAHEDRON-ASYMMETR, V25, P334
[10]   Catalytic asymmetric Henry reaction [J].
Boruwa, Joshodeep ;
Gogoi, Naminita ;
Saikia, Partha Pratim ;
Barua, Nabin C. .
TETRAHEDRON-ASYMMETRY, 2006, 17 (24) :3315-3326