Aerosol route synthesis of Ni-CeO2-Al2O3 hybrid nanoparticle cluster for catalysis of reductive amination of polypropylene glycol

2019 ◽  
Vol 30 (10) ◽  
pp. 2293-2298 ◽  
Author(s):  
Hung-Yen Chang ◽  
Guan-Hung Lai ◽  
De-Hao Tsai
RSC Advances ◽  
2020 ◽  
Vol 10 (73) ◽  
pp. 45159-45169
Author(s):  
Kyungjun Kim ◽  
Dong Woo Kang ◽  
Youngheon Choi ◽  
Wanggyu Kim ◽  
Hyunjoo Lee ◽  
...  

Addition of Pd into Co helped remarkably to reduce cobalt oxide and nitride to cobalt metal by enhanced hydrogen dissociation and desorption.


2019 ◽  
Vol 127 ◽  
pp. 15-19 ◽  
Author(s):  
Hung-Yen Chang ◽  
Guan-Hung Lai ◽  
Chih-Yuan Lin ◽  
Chun-Yu Lee ◽  
Chih-Cheng Chia ◽  
...  

2018 ◽  
Vol 568 ◽  
pp. 114-122 ◽  
Author(s):  
Kyungjun Kim ◽  
Youngheon Choi ◽  
Hyunjoo Lee ◽  
Jae W. Lee

Langmuir ◽  
2018 ◽  
Vol 34 (17) ◽  
pp. 5030-5039 ◽  
Author(s):  
Li-Ting Chen ◽  
Ung-Hsuan Liao ◽  
Je-Wei Chang ◽  
Shih-Yuan Lu ◽  
De-Hao Tsai

2020 ◽  
Author(s):  
Bapurao Bhoge ◽  
Ishu Saraogi

Chemo- and site-specific modifications in oligonucleotides have wide applicability as mechanistic probes in chemical biology. Here we have employed a classical reaction in organic chemistry, reductive amination, to selectively functionalize the N<sup>2</sup>-amine of guanine/2’-deoxyguanine monophosphate. This method specifically modifies guanine in several tested DNA oligonucleotides, while leaving the other bases unaffected. Using this approach, we have successfully incorporated desired handles chemoselectively into DNA oligomers.


Author(s):  
Jack Rowbotham ◽  
Oliver Lenz ◽  
Holly Reeve ◽  
Kylie Vincent

<p></p><p>Chemicals labelled with the heavy hydrogen isotope deuterium (<sup>2</sup>H) have long been used in chemical and biochemical mechanistic studies, spectroscopy, and as analytical tracers. More recently, demonstration of selectively deuterated drug candidates that exhibit advantageous pharmacological traits has spurred innovations in metal-catalysed <sup>2</sup>H insertion at targeted sites, but asymmetric deuteration remains a key challenge. Here we demonstrate an easy-to-implement biocatalytic deuteration strategy, achieving high chemo-, enantio- and isotopic selectivity, requiring only <sup>2</sup>H<sub>2</sub>O (D<sub>2</sub>O) and unlabelled dihydrogen under ambient conditions. The vast library of enzymes established for NADH-dependent C=O, C=C, and C=N bond reductions have yet to appear in the toolbox of commonly employed <sup>2</sup>H-labelling techniques due to requirements for suitable deuterated reducing equivalents. By facilitating transfer of deuterium atoms from <sup>2</sup>H<sub>2</sub>O solvent to NAD<sup>+</sup>, with H<sub>2</sub> gas as a clean reductant, we open up biocatalysis for asymmetric reductive deuteration as part of a synthetic pathway or in late stage functionalisation. We demonstrate enantioselective deuteration via ketone and alkene reductions and reductive amination, as well as exquisite chemo-control for deuteration of compounds with multiple unsaturated sites.</p><p></p>


2013 ◽  
pp. 215-218
Author(s):  
Robert O. Hatch ◽  
Craig M. Giles ◽  
Jay S. Creiglow ◽  
David R. Smith

The use of sodium propylene glycol for thick juice storage was investigated at Spreckels Sugar Company, in Brawley, California (USA). Sodium-polypropylene glycol has a density of 1.07 and does not mix with thick juice. Therefore it is suitable as a barrier layer. Chemical properties of propylene glycol, and the deposition on the top of thick juice are described. First results of the last campaign are compared with data from previous years. A significantly lower tendency in the reduction of the quality of the thick juice was found.


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