Semi-reduction of alkynes catalyzed by a tri-palladium complex

被引:0
|
作者
Wang, Yu-Hao [1 ]
Liu, Shiuh-Tzung [1 ]
机构
[1] Department of Chemistry, National Taiwan University, Taipei,10617, Taiwan
关键词
D O I
10.1016/j.poly.2024.117276
中图分类号
O62 [有机化学]; TQ [化学工业];
学科分类号
070303 ; 0817 ; 081704 ;
摘要
Upon activation by ammonia-borane, a tri-palladium complex [(bpnp)2Pd3Cl2]Cl2 (Pd3) was found to be catalytically active for hydrogenation of alkynes to render the corresponding cis-olefins. Typically, a mixture of diphenylacetylene (0.80 mmol), Pd3 (0.2 mol %), and NH3.BH3 (10 mol%) in THF/H2O (10:1, 1 mL) was stirred at 30 °C under H2 (1 atm) for 2 h, giving (Z)-stilbene in 95 % yield with a turnover frequency (TOF) ∼240 h−1. This catalyst is applicable to both internal and terminal alkynes with aryl or alkyl substituents. © 2024 Elsevier Ltd
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