Membrane-Grafted Asymmetric Organocatalyst for an Integrated Synthesis-Separation Platform
Membrane-Grafted Asymmetric Organocatalyst for an Integrated Synthesis-Separation Platform
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DOI：
10.1021/acscatal.8b01706
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发表时间：
2018-08-01
期刊：
影响因子：
12.9
通讯作者：
Szekely, Gyorgy
中科院分区：
文献类型：
--
作者：
Didaskalou, Christos;Kupai, Jozsef;Szekely, Gyorgy
In this work we introduce a sustainable membrane-based synthesis separation platform for enantioselective organocatalysis. An azido derivatized cinchona-squaramide bifunctional catalyst was synthesized and subsequently grafted to the surface of a polybenzimidazole-based nanofiltration membrane. The favorable effect of the covalent grafting-due to the change in geometry and increased secondary interactions on the catalytic activity due to conformational changes was confirmed by quantum chemical calculations. Asymmetric Michael and aza-Michael reactions of 1,3-dicarbonyl and indole, pyrazole, and triazole derivatives to beta-nitrostyrene were performed with as high as 99% enantiomeric excess. This report on the enantioselective aza-Michael reaction of pyrazoles and triazoles opens new frontiers in the application of squaramide-based cinchona catalysts. A catalytic membrane cascade reactor was developed for an integrated synthesis purification process allowing at least 98% product and substrate recovery, and quantitative in situ solvent recycling. The sustainability of the synthetic methodology was assessed through E-factor and carbon footprint.
