Periodic Mesoporous Silica-Supported Scandium Triflate as a Robust and Reusable Lewis Acid Catalyst for Carbon–Carbon Coupling Reactions in Water

2013 ◽  
Vol 2 (3) ◽  
pp. 486-492 ◽  
Author(s):  
Mingzhen Chen ◽  
Chao Liang ◽  
Fang Zhang ◽  
Hexing Li
2014 ◽  
Vol 16 (8) ◽  
pp. 3768-3777 ◽  
Author(s):  
Fang Zhang ◽  
Xiaotao Wu ◽  
Chao Liang ◽  
Xiaoyan Li ◽  
Zhen Wang ◽  
...  

A multifunctional magnetic mesoporous silica supported Yb(OTf)3 composite was demonstrated to be an efficient and easily recyclable catalyst for the Mukaiyama–Aldol reaction in water.


2020 ◽  
Vol 22 (5) ◽  
pp. 1754-1762 ◽  
Author(s):  
Erlen Y. C. Jorge ◽  
Carolina G. S. Lima ◽  
Thiago M. Lima ◽  
Lucas Marchini ◽  
Manoj B. Gawande ◽  
...  

Lignocellulosic biomass is becoming a viable alternative or a complementary source for obtaining petroleum-derived products such as fuels, polymers and fine chemicals, among others.


2018 ◽  
Vol 26 (1) ◽  
pp. 261-269 ◽  
Author(s):  
Zhuxiu Zhang ◽  
Mengnan Hu ◽  
Qiumin Mei ◽  
Jihai Tang ◽  
Zhaoyang Fei ◽  
...  

2018 ◽  
Vol 14 ◽  
pp. 1595-1618 ◽  
Author(s):  
Yuichi Yoshimura ◽  
Hideaki Wakamatsu ◽  
Yoshihiro Natori ◽  
Yukako Saito ◽  
Noriaki Minakawa

To synthesize nucleoside and oligosaccharide derivatives, we often use a glycosylation reaction to form a glycoside bond. Coupling reactions between a nucleobase and a sugar donor in the former case, and the reaction between an acceptor and a sugar donor of in the latter are carried out in the presence of an appropriate activator. As an activator of the glycosylation, a combination of a Lewis acid catalyst and a hypervalent iodine was developed for synthesizing 4’-thionucleosides, which could be applied for the synthesis of 4’-selenonucleosides as well. The extension of hypervalent iodine-mediated glycosylation allowed us to couple a nucleobase with cyclic allylsilanes and glycal derivatives to yield carbocyclic nucleosides and 2’,3’-unsaturated nucleosides, respectively. In addition, the combination of hypervalent iodine and Lewis acid could be used for the glycosylation of glycals and thioglycosides to produce disaccharides. In this paper, we review the use of hypervalent iodine-mediated glycosylation reactions for the synthesis of nucleosides and oligosaccharide derivatives.


ChemInform ◽  
2003 ◽  
Vol 34 (46) ◽  
Author(s):  
Pentlavalli Sreekanth ◽  
Sang-Wook Kim ◽  
Taegwhan Hyeon ◽  
B. Moon Kim

2003 ◽  
Vol 345 (8) ◽  
pp. 936-938 ◽  
Author(s):  
Pentlavalli Sreekanth ◽  
Sang-Wook Kim ◽  
Taegwhan Hyeon ◽  
B. Moon Kim

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