Synthesis of Diarylmethanes through Palladium-Catalyzed Coupling of Benzylic Phosphates with Arylsilanes
摘要:
An efficient approach to the benzylation of arenes has been developed. The reactions described provide straightforward access to diarylmethanes through Pd-catalyzed coupling of benzylic phosphates with arylsilanes in good to excellent yields. The reaction tolerates a wide range of functionalities such as halide, alkoxyl, and nitro groups.
Palladium/Xiao‐Phos‐Catalyzed Kinetic Resolution of
<i>sec</i>
‐Phosphine Oxides by
<i>P</i>
‐Benzylation
作者:Qiang Dai、Lu Liu、Junliang Zhang
DOI:10.1002/anie.202111957
日期:2021.12.20
rac-secondary phosphine oxides via the enantioselective P-benzylation process catalyzed by the palladium/Xiao-Phos was designed. Both, tert- and sec-phosphine oxides were delivered in good yield and excellent enantiopurity (selectivity factor up to 226.1). The synthetic utilities are further demonstrated by the facile preparation of several P-chiral compounds, precursors of bidentate ligands, and transition
in good to high yields by coupling N-tosylhydrazones (NTHs) with benzylic phosphates as electrophilic partners. The obtained new catalytic system consisted of PdCl2(CH3CN)2/dppp, LiOtBu as a base, and cyclopentyl methyl ether as a green solvent. In addition, we performed a gram-scale transformation using NTH derivatives and benzylic phosphates having a C sp2–Cl bond. The latter was used as a starting
该研究表明,通过将N-甲苯磺酰腙 (NTH) 与磷酸苄基作为亲电伙伴偶联,可以以良好至高产率获得各种具有高化学选择性的二取代和三取代烯烃。得到的新型催化体系由PdCl 2 (CH 3 CN) 2 /dppp、LiO t Bu为碱、环戊基甲基醚为绿色溶剂组成。此外,我们使用 NTH 衍生物和具有 C sp 2 -Cl 键的苄基磷酸酯进行了克级转化。后者被用作关键中间体进一步后功能化的起点。
Photochemistry of phosphate esters: an efficient method for the generation of electrophiles
作者:Richard S. Givens、Bogdan Matuszewski、Phillip S. Athey、M. Robert Stoner