Search results for "Acetone"
showing 10 items of 350 documents
Species-Specific Antioxidant Power and Bioactive Properties of the Extracts Obtained from Wild Mediterranean Calendula Spp. (Asteraceae)
2019
In this study we focused on four taxa of the genus Calendula (C. maritima, C. suffruticosa subsp. fulgida, C. arvensis, and the hybrid between the first two ones), collected in Mediterranean area (Sicily). Six extracts for each species were obtained using solvents with increasing polarity (hexane, ethanol 80%, acetone 70%, and water) and through extraction by supercritical fluids (SFE). It has been observed that the solvent with the highest extraction efficiency was ethanol 80% for all species. However, SFE extracts showed high antioxidant activity comparable to the ethanol 80% extract (polyphenol, DPPH, and reducing power method). These findings were confirmed by in vitro analysis (MTT ass…
CCDC 270841: Experimental Crystal Structure Determination
2005
Related Article: J.-P.Costes, S.Shova, J.M.C.Juan, N.Suet|2005|Dalton Trans.||2830|doi:10.1039/b506102d
CCDC 1584240: Experimental Crystal Structure Determination
2018
Related Article: I. Casanova, M. L. Durán, J. Viqueira, A. Sousa-Pedrares, F. Zani, J. A. Real, J. A. García-Vázquez|2018|Dalton Trans.|47|4325|doi:10.1039/C8DT00532J
CCDC 962935: Experimental Crystal Structure Determination
2014
Related Article: Ilya S. Krytchankou, Dmitry V. Krupenya, Antti J. Karttunen, Sergey P. Tunik, Tapani A. Pakkanen, Pi-Tai Chou, Igor O. Koshevoy|2014|Dalton Trans.|43|3383|doi:10.1039/C3DT52658E
CCDC 1856808: Experimental Crystal Structure Determination
2018
Related Article: Miguel Clemente Leon, Víctor García-López, Mario Palacios-Corella, Alexandre Abhervé, Isaac Pellicer-Carreño, Cédric Desplanches, Eugenio Coronado|2018|Dalton Trans.|47|16958|doi:10.1039/C8DT03511C
CCDC 1856811: Experimental Crystal Structure Determination
2018
Related Article: Miguel Clemente Leon, Víctor García-López, Mario Palacios-Corella, Alexandre Abhervé, Isaac Pellicer-Carreño, Cédric Desplanches, Eugenio Coronado|2018|Dalton Trans.|47|16958|doi:10.1039/C8DT03511C
CCDC 1425262: Experimental Crystal Structure Determination
2016
Related Article: T. Mäkelä, K. Rissanen|2016|Dalton Trans.|45|6481|doi:10.1039/C6DT00414H
CCDC 771545: Experimental Crystal Structure Determination
2011
Related Article: C.J.Adams, J.A.Real, R.E.Waddington|2010|CrystEngComm|12|3547|doi:10.1039/c0ce00149j
CCDC 1944600: Experimental Crystal Structure Determination
2019
Related Article: Víctor García-López, Mario Palacios-Corella, Salvador Cardona-Serra, Miguel Clemente-León, Eugenio Coronado|2019|Chem.Commun.|55|12227|doi:10.1039/C9CC05988A
Synthesis of α-aminonitriles using aliphatic nitriles, α-amino acids, and hexacyanoferrate as universally applicable non-toxic cyanide sources
2018
In cyanation reactions, the cyanide source is often directly added to the reaction mixture, which restricts the choice of conditions. The spatial separation of cyanide release and consumption offers higher flexibility instead. Such a setting was used for the cyanation of iminium ions with a variety of different easy-to-handle HCN sources such as hexacyanoferrate, acetonitrile or α-amino acids. The latter substrates were first converted to their corresponding nitriles through oxidative decarboxylation. While glycine directly furnishes HCN in the oxidation step, the aliphatic nitriles derived from α-substituted amino acids can be further converted into the corresponding cyanohydrins in an oxi…