18 research outputs found
Tools and techniques for solvent selection: green solvent selection guides
Driven by legislation and evolving attitudes towards environmental issues, establishing green solvents for extractions, separations, formulations and reaction chemistry has become an increasingly important area of research. Several general purpose solvent selection guides have now been published with the aim to reduce use of the most hazardous solvents. This review serves the purpose of explaining the role of these guides, highlighting their similarities and differences. How they can be used most effectively to enhance the greenness of chemical processes, particularly in laboratory organic synthesis and the pharmaceutical industry, is addressed in detail
A novel dihydrodifuropyridine scaffold derived from ketones and the chitin-derived heterocycle 3-acetamido-5-acetylfuran
Green approach to synthesis of new series of 6,8a-dihydropyrido[2,3-d]pyrimidine derivatives
Transformation of dl Limonene into Aromatic Compounds Using Supported Heteropolyacid Catalysts
International audienceThe transformation of DL limonene (mixture of D- and L-form ~ 1:1) that came from the pyrolysis of scrap tires rubber was studied using four heteropolyacid catalysts (H3PW12O40, H3PMo12O40, H4SiW12O40 and H4PMo11VO40) supported on Q-10, SBA-15, MCM-41, and KIT-6. The catalyst activity was measured using a py/GC/FID under a nitrogen atmosphere. The active phase and support were characterized using various technical methods (XRD, Raman, TEM, N2 adsorption–desorption, NH3-TPD, and py-FTIR). The highest weak acidity and largest number of Lewis acid sites promoted the conversion of DL limonene. The isomerization reactions seemed to be more favored than disproportionation reactions. The p-cymene yield was favored, with a high weak acidity and high Lewis/Brønsted acid sites ratio. Moreover, the results show that the use of amorphous support with a higher pore size seems to promote the conversion of DL limonene and the production of p-cymene