An attempt to provide an environmentally friendly solvent selection guide for olefin metathesis
Literature Information
Krzysztof Skowerski, Jacek Białecki, Andrzej Tracz, Tomasz K. Olszewski
A range of environmentally conservative solvents was evaluated for application in olefin metathesis. Different commercially available and most frequently applied ruthenium catalysts were employed. The data obtained can be used as a guide to facilitate replacement of environmentally detrimental chlorinated or aromatic solvents with greener reaction media in order to make applications of olefin metathesis in both industry and academia more environmentally benign and sustainable processes.
Related Literature
A rainbow ratiometric fluorescent sensor array on bacterial nanocellulose for visual discrimination of biothiols
Samira Abbasi-Moayed, Hamed Golmohammadi, Arafeh Bigdeli
DOI: 10.1039/C8AN00637G
Correction: Quantification of isomerically summed hydrocarbon contributions to crude oil by carbon number, double bond equivalent, and aromaticity using gas chromatography with tunable vacuum ultraviolet ionization
Jeremy A. Nowak, Robert J. Weber
DOI: 10.1039/C9AN90049G
A ZnS quantum dot-based super selective fluorescent chemosensor for soluble ppb-level total arsenic [As(iii) + As(v)] in aqueous media: direct assay utilizing aggregation-enhanced emission (AEE) for analytical application
Saurav Kayal, Mintu Halder
DOI: 10.1039/C9AN00516A
On-line detection of radioactive and non-radioactive heavy metals in tobacco smoke using portable laser-induced breakdown spectroscopy
Pengfei Zhang, Zhixuan Huang, Yiwen Ma, Yang Li, Naqash Ali, Qifeng Li, Da Chen
DOI: 10.1039/C9AN00050J
Bimetallic plasmonic Au@Ag nanocuboids for rapid and sensitive detection of phthalate plasticizers with label-free surface-enhanced Raman spectroscopy
Xiaoyan Hu, Xinru Wang, Zipan Ge, Le Zhang, Yaru Zhou, Jingya Li, Linfeng Bu, Hengan Wu, Pan Li
DOI: 10.1039/C9AN00251K
Enhanced selectivity of target gas molecules through a minimal array of gas sensors based on nanoparticle-decorated SWCNTs
Sonia Freddi, Giovanni Drera, Stefania Pagliara, Andrea Goldoni, Luigi Sangaletti
DOI: 10.1039/C9AN00551J
Multi-functional derivatization of amine, hydroxyl, and carboxylate groups for metabolomic investigations of human tissue by electrospray ionization mass spectrometry
Tianjiao Huang, Richard Lee, Dawn S. Hui, James L. Edwards
DOI: 10.1039/C8AN00490K
Flexible plasmonic graphene oxide/heterostructures for dual-channel detection
Varnika Prakash, Raul D. Rodriguez, Ammar Al-Hamry, Anna Lipovka, Elena Dorozhko, Oleksandr Selyshchev, Bing Ma, Shweta Sharma, Surinder K. Mehta, Ashutosh Mukherjee, Dietrich R. T. Zahn, Olfa Kanoun, Evgeniya Sheremet
DOI: 10.1039/C8AN02495B
Design of Gaussia luciferase-based bioluminescent stem-loop probe for sensitive detection of HIV-1 nucleic acids
Hamdi Joda, Geoffrey Stone, Sylvia Daunert, Sapna Deo
DOI: 10.1039/C8AN00047F
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
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.











![Imidazo[1,2-c]pyrimidine structure Imidazo[1,2-c]pyrimidine structure](https://static.chemtradehub.com/structs/274/274-78-2-8b4c.webp)
![N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure](https://static.chemtradehub.com/structs/142/1426944-49-1-1e4c.webp)
![6-Bromo-3-ethyl-3H-imidazo[4,5-b]pyridine structure 6-Bromo-3-ethyl-3H-imidazo[4,5-b]pyridine structure](https://static.chemtradehub.com/structs/103/1033202-59-3-2a8f.webp)
