Towards resource efficient chemistry: tandem reactions with renewables

Literature Information

Publication Date 2013-11-29
DOI 10.1039/C3GC41960F
Impact Factor 10.182
Authors

Arno Behr, Andreas J. Vorholt, Karoline A. Ostrowski, Thomas Seidensticker


View Original

Abstract

In an economically expanding world new sustainable concepts have to be developed in order to overcome growing problems of resource availability. Merging different “Green principles” is a promising concept in this respect, e.g. the combination of tandem reactions and renewables. This review summarizes the trends in this field and demonstrates advantages and future demands. Four reactions, namely metathesis, hydroformylation, defunctionalisation and isomerisation, have been identified for transforming renewables in tandem reactions. Every reaction yields a reactive intermediate or secures a tailored selectivity in order to use the natural molecular structure of renewables.

Related Literature

The evolution of the surface of the mineral schreibersite in prebiotic chemistry

Nikita L. La Cruz, Danna Qasim, Heather Abbott-Lyon, Claire Pirim, Aaron D. McKee, Thomas Orlando, Maheen Gull, Danny Lindsay, Matthew A. Pasek

2016-05-04 Paper

DOI: 10.1039/C6CP00836D

Hole-transfer induced energy transfer in perylene diimide dyads with a donor–spacer–acceptor motif

Patrick Kölle, Igor Pugliesi, Heinz Langhals, Roland Wilcken, Andreas J. Esterbauer, Regina de Vivie-Riedle, Eberhard Riedle

2015-08-24 Paper

DOI: 10.1039/C5CP02981C

The oxidation of copper catalysts during ethylene epoxidation

M. T. Greiner, T. E. Jones, B. E. Johnson, T. C. R. Rocha, Z. J. Wang, M. Armbrüster, M. Willinger, A. Knop-Gericke, R. Schlögl

2015-08-28 Paper

DOI: 10.1039/C5CP03722K

Quantum mechanical study of the β- and δ-lyase reactions during the base excision repair process: application to FPG

Shahin Sowlati-Hashjin, Stacey D. Wetmore

2015-09-02 Paper

DOI: 10.1039/C5CP04250J

Phosphoryl transfer reaction catalyzed by membrane diacylglycerol kinase: a theoretical mechanism study

Yafei Jiang, Hongwei Tan, Jimin Zheng, Xichen Li, Guangju Chen, Zongchao Jia

2015-08-24 Paper

DOI: 10.1039/C5CP03342J

Effect of Ca2+ codoping on the Eu2+ luminescence properties in the Sr2Si5N8 host lattice: a theoretical approach

Claudio Bulloni, Amador García-Fuente, Werner Urland, Claude Daul

2015-09-07 Paper

DOI: 10.1039/C5CP02915E

An advanced approach for measuring acidity of hydroxyls in confined space: a FTIR study of low-temperature CO and 15N2 adsorption on MOF samples from the MIL-53(Al) series

M. Mihaylov, S. Andonova, K. Chakarova, A. Vimont, E. Ivanova, N. Drenchev, K. Hadjiivanov

2015-08-17 Paper

DOI: 10.1039/C5CP04139B

Thermoelectric performance enhancement of Mg2Sn based solid solutions by band convergence and phonon scattering via Pb and Si/Ge substitution for Sn

Binghui Ge, Qing Jie, Udara Saparamadu, Weishu Liu, Zhifeng Ren

2016-07-04 Paper

DOI: 10.1039/C6CP03944H

You might also like

Compound Q&A

What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?

When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...

40716-16-34-Methyl-6-(trifluor...
Compound Q&A

What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?

4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...

405058-00-64-(3,5-Difluoropheny...
Compound Q&A

How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?

5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...

338982-07-35-{[4-(Trifluorometh...
Compound Q&A

What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?

The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...

6317-57-34-Benzylaniline hydr...
Compound Q&A

Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?

[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...

871329-58-7[3-(Diethylsulfamoyl...
Compound Q&A

What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?

3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...

115929-62-93-Bromo-2,5-dimethox...
Compound Q&A

What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?

N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...

915922-67-7N-Methyl-1-(5-methyl...
Compound Q&A

What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?

This compound is primarily used in the pharmaceutical industry for the synthesis...

24828-96-4Carbamic acid, N-[(5...
Compound Q&A

How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?

2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...

1298101-47-92-Methyl-2-propanyl ...
Compound Q&A

What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?

Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...

367-33-9Ethyl 2-bromo-4,4,4-...

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 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.