首页> 外文期刊>The Journal of Organic Chemistry >Enantioselective fluorination of tert-butoxycarbonyl lactones and lactams catalyzed by chiral Pd(II)-bisphosphine complexes
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Enantioselective fluorination of tert-butoxycarbonyl lactones and lactams catalyzed by chiral Pd(II)-bisphosphine complexes

机译:手性Pd(II)-双膦配合物催化叔丁氧羰基内酯和内酰胺的对映选择性氟化

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摘要

An efficient catalytic enantioselective fluorination of tert-butoxycarbonyl lactones and lactams is reported. Reactions of the lactone substrates proceeded smoothly in an alcoholic solvent with a catalytic amount of chiral Pd(II) complex. In the case of the less acidic lactam substrates, concurrent use of the Pd complex and 2,6-lutidine as a cocatalyst was effective. Under the reaction conditions, the fluorinated lactones and lactams were obtained in good yield with excellent enantioselectivity (94-99% ee).
机译:报道了叔丁氧羰基内酯和内酰胺的有效催化对映选择性氟化。内酯底物的反应在具有催化量的手性Pd(II)配合物的醇溶剂中顺利进行。在酸性较低的内酰胺底物的情况下,同时使用Pd配合物和2,6-lutidine作为助催化剂是有效的。在反应条件下,以良好的收率和优异的对映选择性(94-99%ee)获得氟化内酯和内酰胺。

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