Fe3O4nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine

Literature Information

Publication Date 2010-01-13
DOI 10.1039/B920000B
Impact Factor 10.182
Authors

Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song, Chao-Jun Li


View Original

Abstract

A robust, safe and magnetically recoverable Fe3O4 nanoparticle catalyzed three-component coupling of aldehyde, alkyne, and amine (A3-coupling) was developed. A diverse range of propargylamines were obtained in moderate to high yield under mild conditions in air. The separation and reuse of the magnetic Fe3O4 nanoparticles were very simple, effective and economical.

Related Literature

Functionalisation of MWCNTs with poly(lauryl acrylate) polymerised by Cu(0)-mediated and RAFT methods

Jaipal Gupta, Daniel J. Keddie, Chaoying Wan, David M. Haddleton, Tony McNally

2016-05-12 Paper

DOI: 10.1039/C6PY00522E

In situ synthesis of thermo-responsive ABC triblock terpolymer nano-objects by seeded RAFT polymerization

Yaqing Qu, Fei Huo, Quanlong Li, Xin He, Shentong Li, Wangqing Zhang

2014-05-30 Paper

DOI: 10.1039/C4PY00510D

Synthesis of nanoscaled poly(styrene-co-n-butyl acrylate)/silica particles with dumbbell- and snowman-like morphologies by emulsion polymerization

Lucie Malosse, Etienne Duguet, Muriel Lansalot, Elodie Bourgeat-Lami, Serge Ravaine

2014-06-05 Paper

DOI: 10.1039/C4PY00370E

Vesicles of double hydrophilic pullulan and poly(acrylamide) block copolymers: a combination of synthetic- and bio-derived blocks

Jochen Willersinn, Anna Bogomolova, Marc Brunet Cabré, Bernhard V. K. J. Schmidt

2017-01-09 Paper

DOI: 10.1039/C6PY02212J

Highly thermal conductive resins formed from wide-temperature-range eutectic mixtures of liquid crystalline epoxies bearing diglycidyl moieties at the side positions

Hyeonuk Yeo, Nam-Ho You, Se Gyu Jang, Seokhoon Ahn, Kwang-Un Jeong, Seung Hee Lee, Munju Goh

2017-04-05 Paper

DOI: 10.1039/C7PY00243B

Facile one-pot access to π-conjugated polymers via sequential bromination/direct arylation polycondensation

Hitoshi Saito, Jieran Chen, Junpei Kuwabara, Takeshi Yasuda, Takaki Kanbara

2017-04-25 Paper

DOI: 10.1039/C7PY00332C

6-Oxoverdazyl radical polymers with tunable electrochemical properties

2014-07-04 Communication

DOI: 10.1039/C4PY00829D

Control over the assembly and rheology of supramolecular networks via multi-responsive double hydrophilic copolymers

Jérémy Brassinne, Charles-André Fustin, Jean-François Gohy

2017-01-30 Paper

DOI: 10.1039/C6PY02143C

Synthesis of highly branched polymers by reversible complexation-mediated copolymerization of vinyl and divinyl monomers

Hongjun Yang, Zhongrui Wang, Yulei Zheng, Wenyan Huang, Xiaoqiang Xue, Bibiao Jiang

2017-02-21 Paper

DOI: 10.1039/C7PY00174F

Innovative well-defined primary amine-based polyacrylates for plasmid DNA complexation

Hien The Ho, Sagrario Pascual, Véronique Montembault, Nathalie Casse, Laurent Fontaine

2014-06-16 Communication

DOI: 10.1039/C4PY00585F

You might also like

Compound Q&A

What regulatory guidelines apply to 4-Amino-3-bromophenol (CAS: 74440-80-5)?

4-Amino-3-bromophenol (CAS: 74440-80-5) falls under the classification of a haza...

74440-80-54-Amino-3-bromopheno...
Compound Q&A

How should (17beta)-3-Oxoestr-4-en-17-yl acetate (CAS: 1425-10-1) be stored?

(17beta)-3-Oxoestr-4-en-17-yl acetate should be stored in a cool, dry place away...

1425-10-1(17beta)-3-Oxoestr-4...
Compound Q&A

What are the physical and chemical properties of 2-[(2,2-Diethoxyethyl)disulfanyl]-1,1-diethoxyethane (CAS: 76505-71-0)?

2-[(2,2-Diethoxyethyl)disulfanyl]-1,1-diethoxyethane (CAS: 76505-71-0) is a colo...

76505-71-02-[(2,2-Diethoxyethy...
Compound Q&A

What is the market or research trend for 1-(β-D-ribofuranosyl)-1H-imidazo[4,5-c]pyridin-4-amine?

The market and research for 1-(β-D-ribofuranosyl)-1H-imidazo[4,5-c]pyridin-4-ami...

6736-58-91-(beta-D-Ribofurano...
Compound Q&A

How should waste containing Conjugated Estrogen (CAS: 12126-59-9) be handled?

Waste containing Conjugated Estrogen (CAS: 12126-59-9) should be collected and d...

12126-59-9Conjugated Estrogen
Compound Q&A

What is the market or research trend for Bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate?

The market for Bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate (CAS...

88738-78-7Bis(2,2,2-trifluoroe...
Compound Q&A

Are there alternatives to 3,4'-Di-O-methylellagic acid (CAS: 57499-59-9) in synthesis?

There are several alternatives to 3,4'-Di-O-methylellagic acid (CAS: 57499-59-9)...

57499-59-93,4'-Di-O-methylella...
Compound Q&A

What regulatory guidelines apply to 2-Chloro-N,N-dimethylpyridin-4-amine (CAS: 59047-70-0)?

2-Chloro-N,N-dimethylpyridin-4-amine (CAS: 59047-70-0) is regulated under the Gl...

59047-70-02-Chloro-N,N-dimethy...
Compound Q&A

What is cerium(3+);oxygen(2-);vanadium(5+) (CAS: 13597-19-8)?

Cerium(3+);oxygen(2-);vanadium(5+) (CAS: 13597-19-8) is a complex inorganic comp...

13597-19-8cerium(3+);oxygen(2-...
Compound Q&A

Is 7-Chloro-1-iodoisoquinoline (CAS: 1203579-27-4) safe?

7-Chloro-1-iodoisoquinoline (CAS: 1203579-27-4) is generally considered safe whe...

1203579-27-47-Chloro-1-iodoisoqu...

Source Journal

Green Chemistry

Green Chemistry
CiteScore: 16.1
Self-citation Rate: 7.5%
Articles per Year: 944

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.