One-pot catalytic conversion of microalgae (Chlorococcum sp.) into 5-hydroxymethylfurfural over the commercial H-ZSM-5 zeolite

2016 ◽  
Vol 18 (2) ◽  
pp. 452-460 ◽  
Author(s):  
J. J. Wang ◽  
Z. C. Tan ◽  
C. C. Zhu ◽  
G. Miao ◽  
L. Z. Kong ◽  
...  

A high yield of HMF is directly obtained from aquatic microalgae over a commercial acidic zeolite under mild conditions. Experimental results reveal that proteins and lipids in microalgal cells benefit the HMF stability in water.

2018 ◽  
Vol 42 (5) ◽  
pp. 271-273 ◽  
Author(s):  
Li-fen Peng ◽  
Jia-ying Lei ◽  
Li Wu ◽  
Zi-long Tang ◽  
Zhi-peng Luo ◽  
...  

Me3Si-/Ph2P(O)-protected ethynes were successfully transformed to unsymmetrical arylethynes via a one-pot Ph2P(O)-deprotection/ [Pd(dppf)Cl2]-catalysed coupling and one-pot Me3Si-deprotection/Sonogashira coupling under mild conditions and in high yield. Unsymmetrical phenylethynes, unsymmetrical extended phenylene ethynylenes and unsymmetrical anthrylethynes were successfully synthesised in good to excellent yields.


2020 ◽  
Vol 56 (22) ◽  
pp. 3309-3312 ◽  
Author(s):  
Yadong Zhang ◽  
Guojian Chen ◽  
Lei Wu ◽  
Ke Liu ◽  
Hu Zhong ◽  
...  

Two-in-one hydroxyl-incorporated imidazolium ionic network was constructed in one-pot quaternization for enhancing synergistic catalytic conversion of CO2 under mild conditions.


2020 ◽  
Vol 5 (9) ◽  
pp. 1791-1797
Author(s):  
Oleg A. Kazantsev ◽  
Ildar R. Arifullin ◽  
Maria V. Savinova ◽  
Alexey P. Sivokhin ◽  
Yevgeniya A. Bol'shakova ◽  
...  

N-(Dibutylaminomethyl)methacrylamide can be easily obtained via a two-stage one-pot Mannich reaction under mild conditions. By-products are practically absent and the monomer can be easily isolated from the reaction mixture with a 96% yield.


RSC Advances ◽  
2018 ◽  
Vol 8 (30) ◽  
pp. 16585-16592 ◽  
Author(s):  
Chengjiang Fang ◽  
Yan Li ◽  
Wenfeng Zhao ◽  
Weibo Wu ◽  
Hu Li ◽  
...  

A high yield of methyl levulinate (82.5%) was achieved from fructose via a one-pot multi-step conversion process using acidic 3-FPYPW as a heterogeneous catalyst.


Synlett ◽  
2018 ◽  
Vol 29 (09) ◽  
pp. 1219-1222
Author(s):  
Nana Xin ◽  
Xiuying Xie ◽  
Chang-Qiu Zhao ◽  
Xianqiang Huang ◽  
Junhong Zhang ◽  
...  

Hydrophosphorylated fullerene derivatives were readily prepared in one step by treating C60 with Ph3– n PCl n (n = 1–3) and ROH (R = H, alkyl). The one-pot reaction could be performed under mild conditions with moderate to good yields. Dichlorophenylphosphine and alcohols exhibited unexpected reactivity towards C60. A possible reaction mechanism involving the formation of P(III)–OH in situ was proposed to explain the experimental results.


ACS Catalysis ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 2846-2864
Author(s):  
Neha Karanwal ◽  
Malayil Gopalan Sibi ◽  
Muhammad Kashif Khan ◽  
Aye Aye Myint ◽  
Beom Chan Ryu ◽  
...  

2020 ◽  
Vol 17 (11) ◽  
pp. 832-836
Author(s):  
Manijeh Nematpour ◽  
Hossein Fasihi Dastjerdi ◽  
Mehdi Jahani ◽  
Sayyed Abbas Tabatabai

A simple and appropriate procedure for the synthesis of quinazoline-2,4(1H,3H)-dione derivatives from isocyanides, aniline and isocyanate via the Cu-catalyzed intramolecular C-H activation reaction is reported. The advantages of this method are one-pot conditions, accessible starting materials- catalyst, high yield of products, and short reaction times. The structures are confirmed spectroscopically (1H- and 13C-NMR, IR and EI-MS) and by elemental analyses.


2019 ◽  
Vol 19 (2) ◽  
pp. 265-275 ◽  
Author(s):  
Faeze Khalili ◽  
Sara Akrami ◽  
Malihe Safavi ◽  
Maryam Mohammadi-Khanaposhtani ◽  
Mina Saeedi ◽  
...  

Background: This paper reports synthesis, cytotoxic activity, and apoptosis inducing effect of a novel series of styrylimidazo[1,2-a]pyridine derivatives. Objective: In this study, anti-cancer activity of novel styrylimidazo[1,2-a]pyridines was evaluated. Methods: Styrylimidazo[1,2-a]pyridine derivatives 4a-o were synthesized through a one-pot three-component reaction of 2-aminopyridines, cinnamaldehydes, and isocyanides in high yield. All synthesized compounds 4a-o were evaluated against breast cancer cell lines including MDA-MB-231, MCF-7, and T-47D using MTT assay. Apoptosis was evaluated by acridine orange/ethidium bromide staining, cell cycle analysis, and TUNEL assay as the mechanism of cell death. Results: Most of the synthesized compounds exhibited more potent cytotoxicity than standard drug, etoposide. Induction of apoptosis by the most cytotoxic compounds 4f, 4g, 4j, 4n, and 4m was confirmed through mentioned methods. Conclusion: In conclusion, these results confirmed the potency of styrylimidazo[1,2-a]pyridines for further drug discovery developments in the field of anti-cancer agents.


2021 ◽  
Vol 170 ◽  
pp. 1070-1080
Author(s):  
Feng Lin ◽  
Yulong Ma ◽  
Yonggang Sun ◽  
Kanghe Zhao ◽  
Tingting Gao ◽  
...  
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