首页> 外文期刊>Chemical Communications >Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to α,β,γ,δ-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups;
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Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to α,β,γ,δ-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups;

机译:钯催化的不饱和1,6-二芳基膦不对称加成到α,β,γ,δ-不饱和磺酸酯上:通过合理选择吸电子基团来控制区域选择性;

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摘要

Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to electron-deficient dienes was developed through rational selection of electron-withdrawing groups on the dienes. Various chiral allylic phosphine derivatives were synthesized in good yields with high enantioselectivity (up to 96% ee).
机译:通过合理选择二烯上的吸电子基团,开发了钯催化的不对称二芳基膦不对称的1,6-加成反应。以高收率和高对映选择性(高达96%ee)合成了各种手性烯丙基膦衍生物。

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  • 来源
    《Chemical Communications》 |2014年第6期|698-700|共3页
  • 作者单位

    School of Pharmacy, East China University of Science and Technology, 130 Meifong Road, Shanghai 200237, China;

    School of Pharmacy, East China University of Science and Technology, 130 Meifong Road, Shanghai 200237, China;

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China;

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