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Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022
Four-coordinate triarylborane synthesis via cascade B-Cl/C-B cross-metathesis and C-H bond borylation
Kai Yang1, Guan Zhang1, Qiuling Song1,2
1Institute of Next Generation Matter Transformation , College of Chemical Engineering , College of Material Sciences Engineering at Huaqiao University , 668 Jimei Boulevard , Xiamen , Fujian 361021 , P. R. China .
Abstract:
To develop a simple and efficient synthetic method for four-coordinate triarylboranes, we herein describe a tandem highly selective B-Cl/C-B cross-metathesis of two of the same or different arylboranes and C-H bond borylation to synthesize four-coordinate triarylboranes with a broad substrate scope. By switching substituent groups of the target molecules, different emission wavelengths can be achieved from 467 nm to 583 nm with aggregation-induced emission (AIE) properties.
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