首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Palladium-catalyzed borylation and Suzuki coupling (BSC) to obtain β-substituted dehydroamino acid derivatives
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Palladium-catalyzed borylation and Suzuki coupling (BSC) to obtain β-substituted dehydroamino acid derivatives

机译:钯催化的硼化和铃木偶联(BSC)获得β-取代的脱氢氨基酸衍生物

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摘要

Several benzo[b]thienyldehydroamino acids were prepared by one-pot palladium-catalyzed borylation and Suzuki coupling (BSC) from bromobenzo[b]thiophenes containing EDG (OMe or Me), as the component to be borylated with pinacolborane, and pure stereoisomers of β-bromodehydroamino acid derivatives. To our knowledge it is the first time that the BSC reaction involves a non aromatic system.
机译:由一锅钯催化的硼酸酯化和Suzuki偶联(BSC),从含有要与戊四硼烷硼化的EDG(OMe或Me)的溴苯并[b]噻吩和纯的立体异构体制得数种苯并[b]噻吩基脱氢氨基酸。 β-溴代氢氢氨基酸衍生物。据我们所知,这是BSC反应首次涉及非芳族体系。

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