OMICS Publishing Group | Full-text | Organosilicon Chemisty: Past, Present and Future

Organosilicon Chemisty: Past, Present and Future

Vladimir Ya. LEE*

Department of Chemistry, University of Tsukuba, Japan

*Corresponding author: Vladimir Ya. LEE Department of Chemistry University of Tsukuba, Japan Tel: 81-29-853-4523 Fax: 81-29-853-6503 E-mail: leevya@chem.tsukuba.ac.jp

OMICS Publishing Group | Full-text | Organosilicon Chemisty: Past, Present and Future:

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A Facile One-Pot Synthesis of 3,5-Disubstituted Isoxazole Derivatives Using Hydroxy (Tosyloxy) Iodobenzene - Jadhav - 2013 - Journal of Heterocyclic Chemistry - Wiley Online Library

A Facile One-Pot Synthesis of 3,5-Disubstituted Isoxazole Derivatives Using Hydroxy (Tosyloxy) Iodobenzene - Jadhav - 2013 - Journal of Heterocyclic Chemistry - Wiley Online Library:

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Highly atom-efficient and chemoselective reduction of ketones in the presence of aldehydes using heterogeneous catalysts - Green Chemistry (RSC Publishing)

Highly atom-efficient and chemoselective reduction of ketones in the presence of aldehydes using heterogeneous catalysts - Green Chemistry (RSC Publishing):

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An alkyl shift « Naturalproductman’s Blog

An alkyl shift « Naturalproductman’s Blog:

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Selecting with Sulfur

Selecting with Sulfur

A method that selects between two products operates simply by changing the oxidation state of sulfur

Read more

http://www.chemistryviews.org/details/news/5173401/Selecting_with_Sulfur.html

Organocatalytic 1,3-dipolar cycloaddition reactions of ketones and azides with water as a solvent

 

Green Chem., 2013, 15,2384-2388
DOI: 10.1039/C3GC41126E, Communication

Dwun Kit Jonathan Yeung,^a   Tao Gao,^b   Jiayao Huang,^a  Shaofa Sun,^b   Haibing Guo^b and   Jian Wang*^a

*

Corresponding authors

^a

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore
E-mail: chmwangj@nus.edu.sg ;
Fax: (+)65-6516-1691

^b

HuBei Collaborative Innovation Center of Non-power Nuclear Technology, Hubei University of Science and Technology, Hubei Province, China

Received 12 Jun 2013, Accepted 19 Jul 2013
First published online 22 Jul 2013

We reported an enamine catalyzed strategy to fully promote a 1,3-dipolar cycloaddition to access a vast pool of substituted 1,2,3-triazoles in water.

Graphene oxide as a facile acid catalyst for the one-pot conversion of carbohydrates into 5-ethoxymethylfurfural

Graphene oxide obtained by the Hummers method was discovered to be an efficient and recyclable acid catalyst for the conversion of fructose-based biopolymers into 5-ethoxymethylfurfural (EMF). EMF yields of 92%, 71%, 34% and 66% were achieved when 5-hydroxymethylfurfural (HMF), fructose, sucrose and inulin were used as starting materials, respectively.

Green Chem., 2013, 15,2379-2383
DOI: 10.1039/C3GC41109E, Communication

Hongliang Wang,^ab   Tiansheng Deng,^a   Yingxiong Wang,^a  Xiaojing Cui,^ac   Yongqin Qi,^a   Xindong Mu,^d   Xianglin Hou*^a and  Yulei Zhu*^ac

*

Corresponding authors

^a

Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan, PR China
E-mail: houxl@sxicc.ac.cn ;
Fax: (+86) 351-4041153

^b

University of Chinese Academy of Sciences, Beijing, PR China

^c

State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan, PR China

^d

Key Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, P. R. China

Graphene oxide was used as a facile carbon catalyst for converting renewable carbon sources into the potential biofuel 5-ethoxymethylfurfural.