Highly facile and rapid one-pot synthetic protocol for the formation of Se nanoparticles at ambient conditions with controlled phase and morphology: role of starch and cytotoxic studies

2018 ◽  
Vol 6 (1) ◽  
pp. 015029 ◽  
Author(s):  
Avinash Singh ◽  
Apurav Guleria ◽  
Amit Kunwar ◽  
Suman Neogy ◽  
M C Rath
2021 ◽  
Vol 55 (4) ◽  
pp. 2628-2638
Author(s):  
Zhen Cao ◽  
Hao Li ◽  
Gregory V. Lowry ◽  
Xiaoyang Shi ◽  
Xiangcheng Pan ◽  
...  

ChemInform ◽  
2016 ◽  
Vol 47 (1) ◽  
Author(s):  
Mariateresa Giustiniano ◽  
Valentina Mercalli ◽  
Jussara Amato ◽  
Ettore Novellino ◽  
Gian Cesare Tron
Keyword(s):  
One Pot ◽  

2014 ◽  
Vol 24 (7) ◽  
pp. 727-753 ◽  
Author(s):  
Myoungsun Suh ◽  
Hyoungeun Moon ◽  
Heesup Han ◽  
Sunny Ham
Keyword(s):  

1984 ◽  
Vol 14 (12) ◽  
pp. 1105-1110 ◽  
Author(s):  
Seiki Saito ◽  
Shin-Ichi Hamano ◽  
Masami Inaba ◽  
Toshio Moriwake
Keyword(s):  
One Pot ◽  

Small ◽  
2014 ◽  
Vol 10 (9) ◽  
pp. 1771-1778 ◽  
Author(s):  
Shengrong Ye ◽  
Aaron R. Rathmell ◽  
Yoon-Cheol Ha ◽  
Adria R. Wilson ◽  
Benjamin J. Wiley

2020 ◽  
Author(s):  
Dung Do

<p></p><p>Chiral molecules with their defined 3-D structures are of paramount importance for the study of chemical biology and drug discovery. Having rich structural diversity and unique stereoisomerism, chiral molecules offer a large chemical space that can be explored for the design of new therapeutic agents.<sup>1</sup> In practice, chiral architectures are usually prepared from organometallic and organocatalytic processes where a transition metal or an organocatalyst is tailor-made for a desired reaction. As a result, developing a method that enables rapid assembly of chiral complex molecules under a metal- and organocatalyst-free condition represents a daunting challenge. Here we developed a straightforward one-pot procedure to create a chiral 3-D structure from 2-D structures and an amino acid without any chiral catalyst. The center of this research is the design of a <a>special chiral spiroimidazolidinone cyclohexadienone intermediate</a>, a merger of a chiral reactive substrate with multiple nucleophillic/electrophillic sites and a transient organocatalyst. <a>This unique substrate-catalyst (“sub-catalyst”) dual role of the intermediate was displayed in its aza-Michael/Michael cascade reaction with an </a>α,β-unsaturated aldehyde under an iminium/enamine catalysis. <a>The enhanced co-ordinational proximity of the chiral substrate and catalyst</a> in the transition state resulted in a substantial steric discrimination and an excellent overall diastereoselectivity. Aza-tricylic molecules with six contiguous stereocenters were assembled from <i>N</i>-alkylated aminophenols, α,β-unsaturated aldehydes and chiral α-amino acids under a hidden “sub-catalysis” where the strategically produced “sub-catalyst” does not present in initial components of the reaction. The success of this methodology will pave the way for many efficient preparations of chiral complex molecules.</p><br><p></p>


Processes ◽  
2020 ◽  
Vol 8 (7) ◽  
pp. 774
Author(s):  
Mohammadreza Taheraslani ◽  
Han Gardeniers

Methane is activated at ambient conditions in a dielectric barrier discharge (DBD) plasma reactor packed with Pd/γ-alumina catalyst containing different loadings of Pd (0.5, 1, 5 wt%). Results indicate that the presence of Pd on γ-alumina substantially abates the formation of deposits, leads to a notable increase in the production of alkanes and olefins and additionally improves the energy efficiency compared to those obtained for the non-packed reactor and the bare γ-alumina packed reactor. A low amount of Pd (0.5 and 1 wt%) favors achieving a higher production of olefins (mainly C2H4 and C3H6) and a higher yield of H2. Increasing Pd loading to 5 wt% promotes the interaction of H2 and olefins, which consequently intensifies the successive hydrogenation of unsaturated compounds, thus incurring a higher production of alkanes (mainly C2H6 and C3H8). The substantial abatement of the deposits is ascribed to the role of Palladium in moderating the strength of the electric and shifting the reaction pathways, in the way that hydrogenation reactions of deposits’ precursors become faster than their deposition on the catalyst.


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