Zobrazeno 1 - 10
of 272
pro vyhledávání: '"Rita Annunziata"'
Autor:
Capaci, Piergiorgio, Barozzi, Fabrizio, Forciniti, Stefania, Anglana, Chiara, Iuele, Helena, Accogli, Rita Annunziata, Carra, Angela, Lenucci, Marcello Salvatore, del Mercato, Loretta L., Di Sansebastiano, Gian Pietro
Publikováno v:
Plants (2223-7747); Dec2024, Vol. 13 Issue 24, p3530, 16p
Autor:
Antonio Miceli, Francesca Nicolì, Erika Sabella, Eliana Nutricati, Carmine Negro, Rita Annunziata Accogli, Marzia Vergine, Andrea Luvisi
Publikováno v:
Records of Natural Products, Vol 13, Iss 3, Pp 205-215 (2019)
The purpose of this research was to investigate phytochemical profiles and antioxidant activity in four Salvia species growing in Salento (Southern Italy). The hydrodistillation products obtained from the aerial parts of Salvia clandestina, Salvia fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64f83aca1b6f32d6802644834c9496e2
https://www.acgpubs.org/doc/2019013007525396-RNP-EO-1809-119.pdf
https://www.acgpubs.org/doc/2019013007525396-RNP-EO-1809-119.pdf
Publikováno v:
Molecules, Vol 22, Iss 12, p 2181 (2017)
The formation of novel chiral bidentate phosphoroamides structures able to promote Lewis base-catalyzed Lewis acid-mediated reactions was investigated. Two different classes of phosphoroamides were synthetized: the first class presents a phthalic aci
Externí odkaz:
https://doaj.org/article/06f40f2fdea94601a5fc71a049c16492
Publikováno v:
Catalysis Today. 308:94-101
This work describes the organocatalytic α-trifluoromethylthiolation of silylenol ethers using N-(trifluoromethylthio)saccharin as trifluoromethylthiolating reagent that is activated by the presence of catalytic amounts of a Lewis base. Tetrahydrothi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7461e7638081efdad48e4f77969d730
https://doi.org/10.1016/j.cattod.2017.09.013
https://doi.org/10.1016/j.cattod.2017.09.013
Publikováno v:
Advanced Synthesis & Catalysis. 359:2375-2382
A new class of solid supported chiral imidazolidinones organocatalysts for the catalytic reduction of imines with trichlorosilane was developed. Polystyrene proved to be a more effective support than silica in terms of both chemical and stereochemica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1820d7b166b4df17ce39d2876eb3631
https://doi.org/10.1002/adsc.201700376
https://doi.org/10.1002/adsc.201700376
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Publikováno v:
Synthesis. 47:2113-2124
The stereoselective direct aldol reaction of S-phenyl thioesters and aromatic aldehydes promoted by tetrachlorosilane was realized for the first time; the proposed mechanism involves the formation of a chiral cationic hypervalent silicon species and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d1ff3d6d512e0197def3def0370ea80
https://doi.org/10.1055/s-0034-1379914
https://doi.org/10.1055/s-0034-1379914
Publikováno v:
ChemCatChem. 7:1490-1499
9-Amino-9-deoxy-epi-quinine, properly modified by suitable linkers, was anchored on highly cross-linked polystyrene, poly(ethylene glycol), and silica. The resulting species were characterized by NMR spectroscopy and tested as supported organocatalys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dd6fb3f0c1c4deb21d13bec8dbe34e1
https://doi.org/10.1002/cctc.201500106
https://doi.org/10.1002/cctc.201500106
Publikováno v:
Molecules; Volume 22; Issue 12; Pages: 2181
Molecules, Vol 22, Iss 12, p 2181 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 12, p 2181 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
The formation of novel chiral bidentate phosphoroamides structures able to promote Lewis base-catalyzed Lewis acid-mediated reactions was investigated. Two different classes of phosphoroamides were synthetized: the first class presents a phthalic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4915515e2c4a616deae7ddb32004472b
Publikováno v:
Tetrahedron Letters. 55:6639-6642
Starting from ( E )-β-substituted-β-nitroacrylates and α,β-unsaturated ketones, a stereoselective organocatalyzed one-pot methodology allowed to synthesize highly decorated chiral 2-nitro-cyclohexane carboxylic esters. The reaction is promoted by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3663df8b538a4fdee58f48f1dfad890a
https://doi.org/10.1016/j.tetlet.2014.10.073
https://doi.org/10.1016/j.tetlet.2014.10.073