Supercritical CO2-facilitating large-scale synthesis of CeO2 nanowires and their application for solvent-free selective hydrogenation of nitroarenes

2010 ◽  
Vol 20 (10) ◽  
pp. 1947 ◽  
Author(s):  
Zhenyu Sun ◽  
Hongye Zhang ◽  
Guimin An ◽  
Guanying Yang ◽  
Zhimin Liu
2006 ◽  
Vol 421 (4-6) ◽  
pp. 584-588 ◽  
Author(s):  
Zhengsong Lou ◽  
Changle Chen ◽  
Dejian Zhao ◽  
Shengli Luo ◽  
Zhongchun Li

Molecules ◽  
2018 ◽  
Vol 23 (11) ◽  
pp. 2936 ◽  
Author(s):  
Zhiping Che ◽  
Yuee Tian ◽  
Shengming Liu ◽  
Jia Jiang ◽  
Mei Hu ◽  
...  

A series of 2-alkyl-2-(N-arylsulfonylindol-3-yl)-3-N-acyl-5-aryl-1,3,4-oxadiazolines were expeditious prepared under microwave-assisted, catalyzed by HgCl2 and solvent-free conditions. This method has the advantage of low catalyst loading and recovering catalyst, ease reaction and repaid reaction times, easy separation products and excellent yields, and more conducive to the large-scale synthesis products. Furthermore, compounds 3s, 3y, 3a′, 3b′, 3f′, 3i′, 3q′, and 3r′ exhibited more potent anti-HIV-1 activity with EC50 values of 3.35, 6.12, 3.63, 9.54, 1.79, 0.51, 3.00, and 4.01 μg/mL, and TI values of 32.66, >32.68, 31.22, 13.94, 24.27, 39.59, 26.01, and 24.51, respectively. Especially compound 3i′ displayed the highest anti-HIV-1 activity with TI values of 39.59.


Nano Research ◽  
2021 ◽  
Author(s):  
Hui Ding ◽  
Xuan-Xuan Zhou ◽  
Zi-Hui Zhang ◽  
Yun-Peng Zhao ◽  
Ji-Shi Wei ◽  
...  

2019 ◽  
Author(s):  
Yongzheng Ding ◽  
Shuai Fan ◽  
Xiaoxi Chen ◽  
yuzhen gao ◽  
Gang Li

A Pdᴵᴵ-catalyzed, ligand-enabled gamma-C(sp3)–H arylation of free primary aliphatic amines and amino esters without using an exogenous directing group is reported. This reaction is compatible with unhindered free aliphatic amines, and it is also be applicable to the rapid synthesis of biologically and synthetically valuable unnatural α-amino acids. Large scale synthesis is also feasible using this method.<br>


2019 ◽  
Author(s):  
Alyssa Garreau ◽  
Hanyang Zhou ◽  
Michael Young

<div>Methods to catalytically introduce deuterium in synthetically useful yields ortho to a carboxylic acid directing group on arenes typically requires D2 or CD3CO2D, which makes using these approaches cost prohibitive for large scale synthesis (equipment and reagent costs respectively). Herein we present a simplified approach using catalytic RhIII and D2O as deuterium source, and show its application to H/D exchange on various acidic substrates.</div>


2019 ◽  
Author(s):  
Alyssa Garreau ◽  
Hanyang Zhou ◽  
Michael Young

<div>Methods to catalytically introduce deuterium in synthetically useful yields ortho to a carboxylic acid directing group on arenes typically requires D2 or CD3CO2D, which makes using these approaches cost prohibitive for large scale synthesis (equipment and reagent costs respectively). Herein we present a simplified approach using catalytic RhIII and D2O as deuterium source, and show its application to H/D exchange on various acidic substrates.</div>


2015 ◽  
Vol 12 (2) ◽  
pp. 197-201 ◽  
Author(s):  
Liang Xi ◽  
Di Wu ◽  
Hong-You Zhu ◽  
Cong-Hai Zhang ◽  
Yi Jin ◽  
...  

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