Explore the possible mechanism of this catalytic silylation reaction
Palladium-catalyzed silylation reaction between benzylic halides and silylboronate
3,4
After the successful synthesis of various benzyl silane compounds, we next turned our attention to exploring the possible mechanism of this catalytic silylation reaction. An enantioenriched 2-(chloro(phenyl)methyl)naphthalene was prepared and subjected to this coupling reaction. It was found that the desired silylation product 4 could be obtained in 67% yield and with retention of substrate's enantiopurity.
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