A Solid-Supported Organocatalyst for Continuous-Flow Enantioselective Aldol Reactions

被引:100
作者
Ayats, Carles [1 ]
Henseler, Andrea H. [1 ]
Pericas, Miquel A. [1 ,2 ]
机构
[1] Inst Chem Res Catalonia ICIQ, E-43007 Tarragona, Spain
[2] Univ Barcelona, Dept Quim Organ, E-08028 Barcelona, Spain
关键词
aldol reaction; continuous flow; heterogeneous catalysis; organocatalysis; supported catalysts; 1,3-DIPOLAR CYCLOADDITIONS; ALPHA-AMINOXYLATION; OPTIMIZATION; DERIVATIVES; ALDEHYDES; CATALYST; PROLINE; BATCH;
D O I
10.1002/cssc.201100570
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Asymmetric aldol reactions catalyzed by a novel polystyrene-immobilized proline derivative occur in short reaction times with excellent diastereo- and enantioselectivity. The catalyst can be recovered by simple filtration and shows very high reusability. The high activity depicted by the supported catalyst and its chemical and mechanical stability have allowed its application in packed-bed reactors for continuous flow processing. This system can produce enantio- and diastereomerically pure aldol adducts under continuous flow conditions with a residence time of 26 min. Furthermore, the reactor allowed processing of four different aldol products in sequence without any decrease in both catalytic activity and optical purity. The effective catalyst loading could be reduced to 1.6?% (six-fold reduction of catalyst loading compared to the corresponding batch process).
引用
收藏
页码:320 / 325
页数:6
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