Cascade Knoevenagel condensation-chemoselective transfer hydrogenation catalyzed by Pd nanoparticles stabilized on amine-functionalized aromatic porous polymer

2020 ◽  
Vol 352 ◽  
pp. 298-307 ◽  
Author(s):  
Pillaiyar Puthiaraj ◽  
Kwangsun Yu ◽  
Sung-Hyeon Baeck ◽  
Wha-Seung Ahn
2018 ◽  
Vol 303 ◽  
pp. 227-234 ◽  
Author(s):  
Chinna Krishna Prasad Neeli ◽  
Pillaiyar Puthiaraj ◽  
Yu-Ri Lee ◽  
Young-Min Chung ◽  
Sung-Hyeon Baeck ◽  
...  

ACS Omega ◽  
2018 ◽  
Vol 3 (9) ◽  
pp. 10843-10850 ◽  
Author(s):  
Longkang Zhang ◽  
Xiaotong Liu ◽  
Xin Zhou ◽  
Shutao Gao ◽  
Ningzhao Shang ◽  
...  

2018 ◽  
Vol 449 ◽  
pp. 31-37 ◽  
Author(s):  
Huanhuan Jia ◽  
Yuan Zhao ◽  
Panpan Niu ◽  
Ningyue Lu ◽  
Binbin Fan ◽  
...  

2018 ◽  
Vol 42 (20) ◽  
pp. 16823-16828 ◽  
Author(s):  
Jie Li ◽  
Xin Zhou ◽  
Ning-Zhao Shang ◽  
Cheng Feng ◽  
Shu-Tao Gao ◽  
...  

Well-dispersed Pd nanoparticles supported on nitrogen-enriched porous carbon were prepared and this material displayed excellent catalytic activity for the transfer hydrogenation of alkenes. The Pd@NPC catalyst exhibited high catalytic activity and stability for the hydrogenation of alkenes.


2019 ◽  
Vol 44 (1-2) ◽  
pp. 14-19
Author(s):  
Bilal Nişancı ◽  
Ziya Dağalan

A novel transfer hydrogenation methodology for the reduction of ketones (14 examples) and benzaldehyde derivatives (12 examples) to the corresponding alcohols using Pd nanoparticles supported on mesoporous graphitic carbon nitride (mpg-C3N4/Pd) as a reusable catalyst and ammonia borane as a safe hydrogen source in an aqueous solution MeOH/H2O (v/v = 1/1) is described. The catalytic hydrogenation reactions were conducted in a commercially available high-pressure glass tube at room temperature, and the corresponding alcohols were obtained in high yields in 2–5 min. Moreover, the presented transfer hydrogenation protocol shows partial halogen selectivity with bromo-, fluoro-, and chloro-substituted carbonyl analogs. In addition, the present catalyst can be reused up to five times without losing its efficiency, and scaling-up the reaction enables α-methylbenzyl alcohol to be produced in 90% isolated yield.


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