Abstract
An efficient Pd-catalyzed silylation reaction of benzylic halides with silylboronate is reported. In this reaction, primary and secondary benzylic halides could react well with silylboronates to afford benzylic silanes. This reaction accommodates a broad substrate scope and proceeds smoothly under very mild reaction conditions. The corresponding products could be obtained in moderate to high yields and with stereospecificity.
Original language | English |
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Pages (from-to) | 5609-5612 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 52 |
Issue number | 32 |
DOIs | |
State | Published - 25 Apr 2016 |
Externally published | Yes |