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Pd/mannose promoted tandem cross coupling-nitro reduction: expedient synthesis of aminobiphenyls and aminostilbenes

机译:钯/甘露糖促进串联交叉偶联-硝基还原:氨基联苯和氨基苯乙烯的简便合成

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摘要

The dual role of D-mannose as a ligand for Pd catalyzed cross-coupling, and as a hydrogen source for nitro reduction is demonstrated in a modular cross coupling-nitro reduction sequence. The synthetic utility and generality of this green protocol has been illustrated by the synthesis of 20 aminobiphenyl and 10 aminostilbene derivatives in high yields through a one-pot Suzuki coupling-nitro reduction and a Heck coupling-nitro reduction, respectively, starting from halonitroarenes as substrates.
机译:D-甘露糖作为钯催化的交叉偶联的配体,以及作为硝基还原的氢源的双重作用已在模块化交叉偶联-硝基还原序列中得到证实。该绿色方案的合成用途和普遍性已通过以卤代硝基芳烃为底物,分别通过一锅Suzuki偶联-硝基还原和Heck偶联-硝基还原以高收率合成20个氨基联苯和10个氨基二苯乙烯衍生物得到了说明。 。

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