首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Selective reduction of alkenes,alpha,bet-unsaturated carbonyl compounds,nitroarenes,nitroso compounds,N,N-hydrogenolysis of azo and hydrazo functions as well as simultaneous hydrodehalogenation and reduction of substituted aryl halides over PdMCM-41
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Selective reduction of alkenes,alpha,bet-unsaturated carbonyl compounds,nitroarenes,nitroso compounds,N,N-hydrogenolysis of azo and hydrazo functions as well as simultaneous hydrodehalogenation and reduction of substituted aryl halides over PdMCM-41

机译:通过PdMCM-41选择性还原烯烃,α,bet不饱和羰基化合物,硝基芳烃,亚硝基化合物,偶氮和and的N,N氢解以及同时加氢脱卤和取代的芳基卤化物的还原

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摘要

Chemoselective reductions of alkenes,alpha,beta-unsaturated carbonyl compounds,nitro and nitroso compounds,N,N-hydrogenolysis of azo and hydrazo functions as well as simultaneous reduction and hydrodehalogenation of substituted aryl halides,including bulkier substrates,were achieved by catalytic transfer hydrogenation(CTH)using mesoporous PdMCM-41 catalyst.The yields were practically unaffected upon recycling of the catalyst.Further,the CTH process is accomplished without affecting the reduction of any other reducible functional group.
机译:通过催化转移加氢实现烯烃,α,β-不饱和羰基化合物,硝基和亚硝基化合物的化学选择性还原,偶氮和的N,N-氢解以及同时取代和取代的芳基卤化物的加氢脱卤,包括催化性加氢(CTH)使用中孔PdMCM-41催化剂。产率几乎不受催化剂循环利用的影响。此外,完成CTH工艺时不会影响任何其他可还原的官能团的还原。

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