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Updated: Jan 19, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Pd-Catalyzed Stereoselective 1,2-Aryboration of Alkenylarenes
Penglin Zhang1, Mimi Xing1, Qitao Guan1
1Tianjin Key Laboratory of Molecular Optoelectronic Science, Department of Chemistry, Institute of Molecular Plus , Tianjin University , Weijin Rd. 92 , Tianjin 300072 , China.
Abstract:
The palladium-catalyzed highly regio- and diastereoselective arylboration of alkenylarenes has been developed. This chemistry afforded the benzylic boronic esters with a broad substrate scope, which are valuable synthetic intermediates for organic synthesis. The chiral anion phase-transfer strategy was designed for this transformation to realize the regio-, diastereo-, and enantioselective control of this reaction simultaneously.
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