首页> 外文期刊>The Journal of Organic Chemistry >Darzens Reaction of Acyl Phosphonates with alpha-Bromo Ketones: Selective Synthesis of cis- and trans-Epoxyphosphonates
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Darzens Reaction of Acyl Phosphonates with alpha-Bromo Ketones: Selective Synthesis of cis- and trans-Epoxyphosphonates

机译:酰基膦酸酯与α-溴代酮的Darzens反应:顺式和反式环氧膦酸酯的选择性合成

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摘要

Acyl phosphonates with alpha-halo ketones in the presence of bases at room temperature afford cis- and trans-epoxyphosphonates in good chemical yields and high selectivities using different bases. The diastereoselectivity of this reaction is easily controlled by changing the base. Changing the base from CS2CO3 to DBU changed the diastereomeric ratio (trans/cis) from 3/2 to 9/1. Moreover, the treatment of the trans isomer with DBU showed a complete conversion to the corresponding cis isomer.
机译:在室温下,在碱的存在下,带有α-卤代酮的酰基膦酸酯可提供顺式和反式环氧膦酸酯,化学收率好,使用不同的碱具有很高的选择性。通过改变碱可以容易地控制该反应的非对映选择性。将基数从CS2CO3更改为DBU,将非对映异构体比率(反式/顺式)从3/2更改为9/1。此外,用DBU处理反式异构体显示完全转化为相应的顺式异构体。

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