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Stereoselective Synthesis of (Z)‐Dihomoallylic Phosphonates with Quaternary Carbon Center by Palladium‐Catalyzed Bisallylation of Vinylethyene Carbonates with β‐Ketophosphonates
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2021-02-17 , DOI: 10.1002/ajoc.202100054 Fener Chen 1 , Zhigang Liu 2 , Miaolin Ke 3 , Ke Zhang 2 , Sheng Zuo 2 , Meifen Jiang 2
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2021-02-17 , DOI: 10.1002/ajoc.202100054 Fener Chen 1 , Zhigang Liu 2 , Miaolin Ke 3 , Ke Zhang 2 , Sheng Zuo 2 , Meifen Jiang 2
Affiliation
A palladium‐catalyzed bisallylation of vinylethylene carbonates with β‐ketophosphonates to access to (Z)‐trisubstituted dihomoallylic phosphonates bearing a quaternary carbon center with good regio‐ and stereoselectivity is reported. This operationally simple protocol exhibits excellent functional group tolerance to deliver valuable dihomoallylic phosphonates.
中文翻译:
钯催化乙烯基乙炔碳酸酯与β-酮基膦酸酯的双烯丙基化反应,与季碳中心立体选择性合成(Z)-二烯丙基膦酸酯
据报道,碳酸亚乙烯酯与β-酮膦酸酯进行钯催化的双烯丙基化反应,可制得具有良好区域和立体选择性的带有季碳中心的(Z)-三取代二高芳基膦酸酯。该操作简单的协议显示出出色的官能团耐受性,可提供有价值的二缩水烷基膦酸酯。
更新日期:2021-04-19
中文翻译:
钯催化乙烯基乙炔碳酸酯与β-酮基膦酸酯的双烯丙基化反应,与季碳中心立体选择性合成(Z)-二烯丙基膦酸酯
据报道,碳酸亚乙烯酯与β-酮膦酸酯进行钯催化的双烯丙基化反应,可制得具有良好区域和立体选择性的带有季碳中心的(Z)-三取代二高芳基膦酸酯。该操作简单的协议显示出出色的官能团耐受性,可提供有价值的二缩水烷基膦酸酯。