Contents list
Literature Information
The first page of this article is displayed as the abstract.
Recommended Journals
Related Literature
Two-photon-absorption DNA sensitization via solvated electron production: unraveling photochemical pathways by molecular modeling and simulation
Elise Dumont
DOI: 10.1039/C6CP02592G
How surface reparation prevents catalytic oxidation of carbon monoxide on atomic gold at defective magnesium oxide surfaces
Kai Töpfer, Jean Christophe Tremblay
DOI: 10.1039/C6CP02339H
Preparation of superhydrophobic films based on the diblock copolymer P(TFEMA-r-Sty)-b-PCEMA
DOI: 10.1039/C5CP02751A
A computational study of the quantum transport properties of a Cu–CNT composite
Mahdi Ghorbani-Asl, Paul D. Bristowe, Krzysztof Koziol
DOI: 10.1039/C5CP01470K
Water distribution in a sorption enhanced methanation reactor by time resolved neutron imaging
A. Borgschulte, R. Delmelle, R. B. Duarte, A. Heel, P. Boillat, E. Lehmann
DOI: 10.1039/C5CP07686B
Temperature-dependent dynamic correlations in suspensions of magnetic nanoparticles in a broad range of concentrations: a combined experimental and theoretical study
Alexey O. Ivanov, Vladimir S. Zverev, Ekaterina A. Elfimova, Alexander V. Lebedev, Alexander F. Pshenichnikov
DOI: 10.1039/C6CP02793H
Positional recurrence maps, a powerful tool to de-correlate static and dynamical disorder in distribution maps from molecular dynamics simulations: the case of Nd2NiO4+d
A. Piovano, A. Perrichon, M. Boehm, M. R. Johnson, W. Paulus
DOI: 10.1039/C5CP06464C
Structural phase transition in perovskite metal–formate frameworks: a Potts-type model with dipolar interactions
Mantas Šimėnas, Sergejus Balčiūnas, Mirosław Maçzka, Jūras Banys, Evaldas E. Tornau
DOI: 10.1039/C6CP03414D
Molecular dynamics investigations of regioselectivity of anionic/aromatic substrates by a family of enzymes: a case study of diclofenac binding in CYP2C isoforms
Ying-Lu Cui, Fang Xu
DOI: 10.1039/C6CP01128D
Effect of extended strain fields on point defect phonon scattering in thermoelectric materials
Brenden R. Ortiz, Haowei Peng, Armando Lopez, Philip A. Parilla, Stephan Lany, Eric S. Toberer
DOI: 10.1039/C5CP02174J
You might also like
Is 4-Benzyl-2,2-dimethylmorpholine (CAS: 84761-04-6) safe?
4-Benzyl-2,2-dimethylmorpholine is generally considered safe when handled under ...
What is (5,6-Dimethoxy-3-pyridinyl)boronic acid (CAS: 1346526-61-1)?
(5,6-Dimethoxy-3-pyridinyl)boronic acid is a chemical compound with the molecula...
How is 1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane (CAS: 67875-55-2) typically synthesized?
1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane is synthesized throug...
What are the main uses of (2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid (CAS: 1018818-04-6)?
(2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid is primarily used as a build...
What precautions should be taken when handling 2,3-Dichloroacrylonitrile (CAS: 22410-58-8)?
When handling 2,3-Dichloroacrylonitrile, it is crucial to wear appropriate perso...
How should (S)-1-(o-Tolyl)ethanamine hydrochloride (CAS: 1332832-16-2) be stored?
(S)-1-(o-Tolyl)ethanamine hydrochloride should be stored in a cool, dry place to...
What are the physical and chemical properties of Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8)?
Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8...
What industries use 2-Methyloxazole-5-carbaldehyde (CAS: 885273-42-7)?
2-Methyloxazole-5-carbaldehyde is used in the pharmaceutical industry for the sy...
What is the market or research trend for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxylate (CAS: 389889-82-1)?
The market for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxyla...
Is 1-Butyl-3-methylpyridinium bromide (CAS: 26576-85-2) safe?
1-Butyl-3-methylpyridinium bromide is generally considered safe for laboratory u...
Source Journal
Green Chemistry

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.














![3-({2-[(2R,4S)-4-Fluoro-2-methyl-1-pyrrolidinyl]-2-oxoethyl}amino)-3-methyl-1-(1-pyrrolidinyl)-1-butanone structure 3-({2-[(2R,4S)-4-Fluoro-2-methyl-1-pyrrolidinyl]-2-oxoethyl}amino)-3-methyl-1-(1-pyrrolidinyl)-1-butanone structure](https://static.chemtradehub.com/structs/118/1186426-66-3-b2e9.webp)