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Room-temperature borylation of C(sp3)−H bond enabled by phosphine-silyl ligands
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DOI:10.1016/j.scib.2026.04.070.png)
Abstract
En 中文
This work develops a new class of tunable bidentate P,Si ligands that enable room-temperature, iridium-catalyzed borylation of C–H bonds with high efficiency and broad substrate scope, offering a practical and mild strategy for synthesizing valuable organoboron compounds.
Keywords:
borylation
C–H bond functionalization
iridium catalysis
phosphine-silyl ligands
organoboron compounds
Journal
IF:
21.1
Papers:
4.8K
Citations:
2.2W
