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首页> 外文期刊>Angewandte Chemie >Catalytic Enantioselective Michael Addition of 1-Fluoro- bis(phenylsulfonyl)methane to α,β-Unsaturated Ketones Catalyzed by Cinchona Alkaloids
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Catalytic Enantioselective Michael Addition of 1-Fluoro- bis(phenylsulfonyl)methane to α,β-Unsaturated Ketones Catalyzed by Cinchona Alkaloids

机译:金鸡纳生物碱催化1-氟双(苯磺酰基)甲烷对α,β-不饱和酮的催化对映选择性迈克尔加成反应

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摘要

There is a high demand in both academia and industry for enantiopure fluorine-containing organic molecules because of their unique pharmacological properties. Although their occurrence in natural systems is rare, monofluorinated analogues of biologically active compounds are often evaluated as bioisosteres of the parent molecules. Compounds with monofluoromethyl groups are also important in biological systems.
机译:对映纯含氟有机分子由于其独特的药理特性而在学术界和工业上都有很高的需求。尽管它们在自然系统中的发生很少,但生物活性化合物的单氟化类似物通常被评估为母体分子的生物等排体。具有一氟甲基的化合物在生物系统中也很重要。

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