Front cover
Literature Information
A graphical abstract is available for this content
Recommended Journals

Proceedings of the National Academy of Sciences of the United States of America

Russian Chemical Reviews

Pharmacological Reviews

Journal of Physics and Chemistry of Solids

European Journal of Wood and Wood Products

Israel Journal of Chemistry

Pure and Applied Chemistry

Organic Preparations and Procedures International

Science Progress

Journal of Catalysis
Related Literature
5-Azadibenzo[a,g]corannulene
V. M. Tsefrikas, A. K. Greene, L. T. Scott
DOI: 10.1039/C6QO00831C
Twisted terrylene dyes: synthesis and application in organic solar cells
Wei Jiang, Rui Xin, Bowei Xu, Jianqi Zhang, Zhixiang Wei, Jianhui Hou, Zhaohui Wang
DOI: 10.1039/C7QO00118E
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Kwan Yin Cheung, Shuaijun Yang, Qian Miao
DOI: 10.1039/C6QO00828C
Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives
Maciej Barłóg, Ihor Kulai, Xiaozhou Ji, Nattamai Bhuvanesh, Somnath Dey, Eric Pierre Sliwinski, Hassan S. Bazzi, Lei Fang, Mohammed Al-Hashimi
DOI: 10.1039/C9QO00044E
The synthesis of unsymmetric diamides through Rh-catalyzed selective C–H bond activation of amides with isocyanates
Xiaoli Yu, Duo-Sheng Wang, Zhaojun Xu, Bobin Yang, Dawei Wang
DOI: 10.1039/C6QO00793G
Polymerization of acetylene: polyynes, but not carbyne‡
Dominik Prenzel, Rolf W. Kirschbaum, Wesley A. Chalifoux, Robert McDonald, Michael J. Ferguson, Thomas Drewello
DOI: 10.1039/C6QO00648E
A new water-soluble cavitand with deeper guest binding properties‡
Faiz-Ur Rahman, Yang Yu
DOI: 10.1039/C9QO00049F
Three-component bis-heterocycliation for synthesis of 2-aminobenzo[4,5]thieno[3,2-d]thiazoles
Huawen Huang, Zhonghua Qu, Xiaochen Ji, Guo-Jun Deng
DOI: 10.1039/C8QO01365A
The influence of the central acceptor unit on the optoelectronic properties and photovoltaic performance of A–D–A–D–A-type co-oligomers
Ibrahim Ata, Duško Popovic, Mika Lindén, Amaresh Mishra, Peter Bäuerle
DOI: 10.1039/C7QO00043J
Copper nitrate-mediated chemo- and regioselective annulation from two different alkynes: a direct route to isoxazoles
Yingying Li, Mingchun Gao, Bingxin Liu
DOI: 10.1039/C6QO00704J
You might also like
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...
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...
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 ...
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...
Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?
[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...
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...
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 ...
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...
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...
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...
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.
![(4aR,5S,6R,8aS)-5-[2-(3-Furyl)ethyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid structure (4aR,5S,6R,8aS)-5-[2-(3-Furyl)ethyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid structure](https://static.chemtradehub.com/structs/184/18411-75-1-d4cd.webp)

![2-[(5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraen-1-yloxy]-1,3-propanediol structure 2-[(5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraen-1-yloxy]-1,3-propanediol structure](https://static.chemtradehub.com/structs/222/222723-55-9-0348.webp)

