Carbonylative Suzuki Coupling Reaction Catalyzed by a Hydrospirophosphorane Palladium Complex
作者:Przemysław Wójcik、Labrini Sygellou、Andrzej Gniewek、Anna Skarżyńska、Anna Trzeciak
DOI:10.1002/cctc.201700946
日期:2017.12.8
A Pd complex with the H‐spirophosphorane ligand, PdCl2P(OCMe2CMe2O)OC6H4NH2} (Cat. 1), was used as the catalyst in the carbonylative Suzuki coupling of substituted iodobenzenes with arylboronic acids and with sodium tetraphenylborate. Substituted diarylketones were obtained in good to excellent yields and a selectivity over 95 % under 1 atm of CO with 1.5 mol % of the catalyst. The promoting role
在取代的碘代苯与芳基硼酸的羰基化铃木偶联反应中,使用具有H-螺磷烷配体PdCl 2 P(OCMe 2 CMe 2 O)OC 6 H 4 NH 2 } (类别1)的Pd络合物作为催化剂。和四苯硼酸钠。得到的二芳基酮的收率好至极好,在1大气压的CO和1.5摩尔%的催化剂下,选择性超过95%。证明了H-螺膦基配体在催化过程中的促进作用。我们使用了X射线光电子能谱,TEM和31P NMR光谱揭示反应期间。图1的化合物经历转变成具有螺磷膦烷配体或通过其脱烷基作用形成的其他P配体的Pd络合物,并转变成Pd纳米颗粒。所有这些Pd种类都有助于提高系统的生产率。