硅烷化
区域选择性
化学
催化作用
齿合度
表面改性
药物化学
有机化学
组合化学
金属
物理化学
作者
Arghya Deb,Sukriti Singh,Kapileswar Seth,Sandeep Pimparkar,Bangaru Bhaskararao,Srimanta Guin,Raghavan B. Sunoj,Debabrata Maiti
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-10-25
卷期号:7 (12): 8171-8175
被引量:113
标识
DOI:10.1021/acscatal.7b03056
摘要
A Pd(II)-catalyzed protocol for highly regioselective distal γ-C–H silylation and germanylation of aliphatic carboxylic acids is reported. Bidentate 8-aminoquinoline as the directing group was found to stabilize the six-membered palladacycle. A variety of aliphatic carboxylic acids and amino acids were silylated and germanylated in good yields and high diasteroselectivities. Detailed mechanistic studies involving isolation of a Pd(II) intermediate, determination of the reaction rate and order, control experiments, and isotopic labeling and DFT studies were found to be crucial for elucidating the elementary steps involved in this distal aliphatic functionalization.
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