Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Emanuela Romio"'
Autor:
Antonella Leggio, Vanessa Leotta, Emilia Lucia Belsito, Maria Luisa Di Gioia, Emanuela Romio, Ilaria Santoro, Domenico Taverna, Giovanni Sindona, Angelo Liguori
Publikováno v:
Chemistry Central Journal, Vol 11, Iss 1, Pp 1-11 (2017)
Abstract This work compares the composition at different temperatures of gaseous phase of bergamot essential oil at equilibrium with the liquid phase. A new GC–MS methodology to determine quantitatively the volatile aroma compounds was developed. T
Externí odkaz:
https://doaj.org/article/c61fa4b8e3b446f597a410876760cdde
Autor:
Domenico Taverna, Giovanni Sindona, Angelo Liguori, Ilaria Santoro, Emilia Lucia Belsito, Maria Luisa Di Gioia, Antonella Leggio, Emanuela Romio, V. Leotta
Publikováno v:
Chemistry Central Journal, Vol 11, Iss 1, Pp 1-11 (2017)
Chemistry Central Journal
Chemistry Central Journal
This work compares the composition at different temperatures of gaseous phase of bergamot essential oil at equilibrium with the liquid phase. A new GC–MS methodology to determine quantitatively the volatile aroma compounds was developed. The adopte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282cdc1b3db86eb5fed23f9708c4ab81
http://link.springer.com/article/10.1186/s13065-017-0340-y
http://link.springer.com/article/10.1186/s13065-017-0340-y
Autor:
V. Leotta, Emanuela Romio, Antonella Leggio, E. L. Belsito, Angelo Liguori, Carlo Siciliano, G. De Luca, M. L. Di Gioia
Publikováno v:
RSC Advances. 6:34468-34475
A one-pot synthesis of secondary and tertiary amides from carboxylic acids and amines by using SOCl2 has been developed. Also when sterically hindered amines were used as the starting materials, excellent yields of the corresponding amides were obtai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff4c4c40fed2c27052c720f740e5fe9a
https://doi.org/10.1039/c5ra24527c
https://doi.org/10.1039/c5ra24527c
Autor:
Emanuela Romio, Angelo Liguori, V. Leotta, Isabella Federica Guarino, Antonella Leggio, Maria Luisa Di Gioia
Publikováno v:
Tetrahedron Letters. 56:5341-5344
A rapid and efficient single-step synthesis of substituted anilines has been developed. The aromatic nitro compounds were reduced by using reducing systems generated by the action of an excess of LiAlH4 on TiCl4. Anilines substituted with different f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3377e872c58852209df9f2a93a0150a
https://doi.org/10.1016/j.tetlet.2015.07.089
https://doi.org/10.1016/j.tetlet.2015.07.089
Autor:
Maria Luisa Di Gioia, Carlo Siciliano, Antonio Tagarelli, Emilia Lucia Belsito, Emanuela Romio, Angelo Liguori, Francesca Malagrinò, Antonella Leggio
Publikováno v:
The Open Food Science Journal. 9:5-13
The present investigation reports a study about the evolution, during ripening, of the fatty acid profile and the fatty acid composition in acylglycerols of three different fermented sausages industrially produced in the Calabria region (Southern Ita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66ba65475be89c6dd10da286d80e1da5
https://doi.org/10.2174/1874256401509010005
https://doi.org/10.2174/1874256401509010005
Autor:
Maria Luisa Di Gioia, Danila Alò, Antonella Leggio, Carlo Siciliano, Emanuela Romio, Emilia Lucia Belsito, Angelo Liguori
Publikováno v:
Journal of Peptide Science. 21:644-650
This work reports an efficient Lewis acid catalysed N-methylation procedure of lipophilic α-amino acid methyl esters in solution phase. The developed methodology involves the use of the reagent system AlCl3/diazomethane as methylating agent and α-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aecfcc0cf23c6b87ecbd80ab92994d2
https://doi.org/10.1002/psc.2777
https://doi.org/10.1002/psc.2777
Autor:
Emanuela Romio, Antonella Leggio, V. Leotta, A. Liguori, Emilia Lucia Belsito, Carlo Siciliano, M. L. Di Gioia
Publikováno v:
Tetrahedron Letters. 56:2062-2066
An expeditious, practical, and mild method for the reduction of amides to amines is reported. The procedure is based on the activation of amides with titanium tetrachloride followed by reduction with lithium aluminum hydride. The reducing system can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c65d8baba92c2e5c59bb67946cff9b0a
https://doi.org/10.1016/j.tetlet.2015.02.074
https://doi.org/10.1016/j.tetlet.2015.02.074
Publikováno v:
RSC Advances. 5:63407-63420
An efficient, solvent-free protocol for the N-fluorenylmethoxycarbonylation and N-benzyloxycarbonylation of amines is described. The reaction of aliphatic and aromatic amines with FmocOSu and Cbz-Osu in [Bmim][BF4] at room temperature afforded the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef28854c6236adbbec8c2c7b1a6ceea0
https://doi.org/10.1039/c5ra12121c
https://doi.org/10.1039/c5ra12121c
Autor:
V. Leotta, Emilia Lucia Belsito, Emanuela Romio, A. Liguori, Carlo Siciliano, Antonella Leggio, M. L. Di Gioia
Publikováno v:
Tetrahedron Letters. 56:199-202
A mild method for the aminolysis of carboxylic acid chlorides to give amides is disclosed. Reactions are carried out in the presence of silver acetate in non-aqueous environments under heterogeneous phase conditions. Amides are easily recovered in ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0448057acbf995603d241f388af6fd5
https://doi.org/10.1016/j.tetlet.2014.11.067
https://doi.org/10.1016/j.tetlet.2014.11.067
Autor:
Maria Luisa Di Gioia, Emanuela Romio, Anna Barattucci, Paola Bonaccorsi, Carlo Siciliano, Andrea Temperini, Lucio Minuti, Antonella Leggio
Publikováno v:
The Journal of Organic Chemistry. 79:5320-5326
A total synthesis of D-erythro-sphinganine [(2S,3R)-2-aminooctadecane-1,3-diol] starting from commercial N-tert-butyloxycarbonyl-L-serine methyl ester is described. The approach is based on the completely stereoselective preparation of an α-amino ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::041afb75453802f5e85025a805c64a72
https://doi.org/10.1021/jo500493c
https://doi.org/10.1021/jo500493c