News and Views
Literature Information
The first page of this article is displayed as the abstract.
Related Literature
Theoretical prediction of silicene as a new candidate for the anode of lithium-ion batteries
Seyedeh Mozhgan Seyed-Talebi, Iraj Kazeminezhad, Javad Beheshtian
DOI: 10.1039/C5CP04666A
A DFT-based comparative equilibrium study of thermal dehydration and hydrolysis of CaCl2 hydrates and MgCl2 hydrates for seasonal heat storage
Amar Deep Pathak, Silvia Nedea, Herbert Zondag, Camilo Rindt, David Smeulders
DOI: 10.1039/C6CP00926C
Improved charge carrier separation in barium tantalate composites investigated by laser flash photolysis
Jenny Schneider, Michael Wark, Roland Marschall
DOI: 10.1039/C5CP07115A
Co-operative motion of multiple benzoquinone disks at the air–water interface
Jennifer E. Satterwhite-Warden, Dilip K. Kondepudi
DOI: 10.1039/C5CP04471E
Computational insights into the inhibition and destabilization of morin on the oligomer of full-length human islet amyloid polypeptide
Qianqian Wang, Shuangyan Zhou, Wei Wei, Zhide Hu
DOI: 10.1039/C5CP03991F
Reproducible, stable and fast electrochemical activity from easy to make graphene on copper electrodes
Zachary P. L. Laker, Jonathan P. Rourke, Neil R. Wilson
DOI: 10.1039/C5CP04070A
A designed lipopeptide with a leucine zipper as an imbedded on/off switch for lipid bilayers
Sijia Wang, Yinxing Shen, Junqi Zhang, Shouhong Xu, Honglai Liu
DOI: 10.1039/C6CP00378H
Branched isomeric 1,2,3-triazolium-based ionic liquids: new insight into structure–property relationships
M. Lartey, J. Meyer-Ilse, J. D. Watkins, E. A. Roth, S. Bowser, V. A. Kusuma, K. Damodaran, M. Haranczyk, E. Albenze, D. R. Luebke, D. Hopkinson, J. B. Kortright
DOI: 10.1039/C5CP04756K
One-pot synthesis of etched Cu2O cubes with exposed {110} facets with enhanced visible-light-driven photocatalytic activity
Linli Tang, Yuhang Du, Chuncai Kong, Shaodong Sun, Zhimao Yang
DOI: 10.1039/C5CP05470B
Molecular analysis of interactions between a PAMAM dendrimer–paclitaxel conjugate and a biomembrane
TianJian Lu
DOI: 10.1039/C5CP02242H
You might also like
What are the main uses of (3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8)?
(3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8) is primari...
What regulatory guidelines apply to 5-(aminomethyl)-2-methoxyphenol (CAS: 89702-89-6)?
5-(Aminomethyl)-2-methoxyphenol (CAS: 89702-89-6) is classified under GHS as a s...
What is Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7)?
Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7) is a heterocyclic organic compo...
Is 1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride (CAS: 1185311-28-7) safe?
1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride is generally ...
What regulatory guidelines apply to [(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2)?
[(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2) is regulated und...
What regulatory guidelines apply to 6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7)?
6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7) falls under the scope of the Glob...
What industries use (2R)-1-(1-Benzofuran-2-yl)-N-propyl-2-pentanamine (CAS: 260550-89-8)?
This compound is primarily used in the pharmaceutical industry for the developme...
What are the main uses of 1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (CAS: 1228013-15-7)?
1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2...
Are there alternatives to {5-(Acryloylamino)-2-[(dimethylamino)methyl]phenyl}boronic acid (CAS: 1217500-78-1) in synthesis?
Alternative reagents such as 2-[(dimethylamino)methyl]phenylboronic acid or rela...
What is 3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2)?
3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2) is an organic compound with the...
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.











![(1R)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one structure (1R)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one structure](https://static.chemtradehub.com/structs/102/10293-06-8-dd8a.webp)


