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natureijƪÎÄÕÂÆäÖÐÒ»¶Î£¬°ïæ·ÒëһϱêºìµÄµØ·½£¬¾¡Á¿¾«È·µã£¬Ç°ºóÎÄÒѾ¸ø³ö£¬·Ç³£¸Ðл![]() Several anilines important for both organic synthesis and industry are densely substituted with a variety of different functional groups. Hence, for a generally applicable catalyst system it is essential to perform the reduction of the nitro group highly chemoselectively. Notably, such functional-group tolerance might also omit the use of protecting groups and streamline more-complex syntheses. Especially with respect to selectivity, the reduction of -NO2 in the presence of other reducible substituents, such as ketones, aldehydes, alkenes or alkynes, remains challenging. Most common commercially available Raney¨Cnickel, palladium or platinum catalysts are troubled by these issues. Nevertheless, Siegrist, Blaser and co-workers achieved the selective reduction of substituted nitroarenes using commercially available platinum catalysts modified by special additives. More recently, another important development came from the group of Corma, who disclosed a heterogeneous gold-based catalyst that can hydrogenate nitro compounds selectively in the presence of a number of functional groups. Nevertheless, so far there exists no inexpensive nonnoble metal catalyst system that allows for a general reduction of all kinds of nitroarenes. |
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