Click chemistry promoted by graphene supported copper nanomaterials-Reference-Cited by-同舟云学术

Click chemistry promoted by graphene supported copper nanomaterials

Published:2014 Issue:97 Volume:50 Page:15374-15377
ISSN:1359-7345
Container-title:Chem. Commun.
language:en
Short-container-title:Chem. Commun.

Author:

Shaygan Nia Ali¹²³⁴⁵,Rana Sravendra¹²³⁴⁵,Döhler Diana¹²³⁴⁵,Noirfalise Xavier⁶⁷,Belfiore Alice⁶⁷,Binder Wolfgang H.¹²³⁴⁵

Affiliation:

1. Institute of Chemistry

2. Chair of Macromolecular Chemistry

3. Faculty of Natural Sciences II (Chemistry, Physics and Mathematics)

4. Martin-Luther University Halle-Wittenberg

5. Halle, Germany

6. Materia Nova Research Center

7. B7000 Mons, Belgium

Abstract

Highly dispersed copper nanoparticles immobilized graphene nanosheets were prepared and used as a recyclable and reusable heterogeneous catalyst with excellent catalytic activity to achieve Cu(i)-catalyzed [3+2] cycloaddition “click” chemistry under both solvent and bulk conditions.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC07774A

Reference33 articles.

1. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

2. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

3. M. T. Meldal and C. W.Tornøe , Proceedings of the Second International and the Seventeenth American Peptide Symposium, 2001, pp. 263–264

4. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

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