An immobilised Co(ii) and Ni(ii) Schiff base magnetic nanocatalyst via a click reaction: a greener approach for alcohol oxidation-Reference-Cited by-同舟云学术

An immobilised Co(ii) and Ni(ii) Schiff base magnetic nanocatalyst via a click reaction: a greener approach for alcohol oxidation

Published:2015 Issue:6 Volume:39 Page:4933-4938
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Bhat Pooja B.¹²³⁴,Bhat Badekai Ramachandra¹²³⁴

Affiliation:

1. Catalysis and Materials Laboratory

2. Department of Chemistry

3. National Institute of Technology Karnataka, Surathkal

4. India

Abstract

A Schiff base immobilised magnetic nanocatalyst synthesized via copper catalysed alkyne azide cycloaddition (CuAAC) exhibited a strong interaction and improved yielding for oxidation of alcohols in a solventless system.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C5NJ00218D

Reference22 articles.

1. Nanoparticle Supported, Magnetically Recoverable Oxodiperoxo Molybdenum Complexes: Efficient Catalysts for Selective Epoxidation Reactions

2. Application of CuAAC for the covalent immobilization of homogeneous catalysts

3. Click on silica: systematic immobilization of Co(ii) Schiff bases to the mesoporous silica via click reaction and their catalytic activity for aerobic oxidation of alcohols

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

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

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