Intranasal dexmedetomidine in pediatrics: update of current knowledge

Autor: Angela Amigoni, Geremia Zito Marinosci, Rosa Puzzutiello, Sergio Picardo, Maria Cristina Mondardini, Francesca Vitale, Paolo Cortellazzi, Alessandra Di Palma, Cristina Navarra, Giorgio Conti, Laura Rinaldi

Publikováno v: Minerva Anestesiologica. 85

Intranasal dexmedetomidine, although still off-label, recently boasted an increasing consensus for different uses, namely, in diagnostic non-painful procedures, in painful procedures and in surgical premedication. However, at present, there is no con

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7412b19b380d57be080a316326188e
https://doi.org/10.23736/s0375-9393.19.13820-5

Biocatalyzed synthesis of enantiomerically enriched β-5-like dimer of 4-vinylphenol

Autor: Sergio Riva, Walter Panzeri, Paolo Gavezzotti, Daniela Monti, Cristina Navarra

Publikováno v: Journal of molecular catalysis. B, Enzymatic
84 (2012): 115–120. doi:10.1016/j.molcatb.2012.03.020
info:cnr-pdr/source/autori:Navarra, Cristina; Gavezzotti, Paolo; Monti, Daniela; Panzeri, Walter; Riva, Sergio/titolo:Biocatalyzed synthesis of enantiomerically enriched beta-5-like dimer of 4-vinylphenol/doi:10.1016%2Fj.molcatb.2012.03.020/rivista:Journal of molecular catalysis. B, Enzymatic (Print)/anno:2012/pagina_da:115/pagina_a:120/intervallo_pagine:115–120/volume:84

The tandem use of laccases and lipases has been exploited for the preparative scale synthesis of enantiomerically enriched dimeric phenols. Laccase-catalyzed oxidation of 4-vinylphenol ( 3 ) in biphasic systems gave as main product the racemic compou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39cf61a98dfdbd5dcd921c625da6d099
https://doi.org/10.1016/j.molcatb.2012.03.020

Laccase-mediated oxidation of phenolic derivatives

Autor: Stephanie G. Burton, Cristina Navarra, Bruno Danieli, Candice M. Goodwin, Sergio Riva

Publikováno v: Journal of Molecular Catalysis B: Enzymatic. 65:52-57

The laccase-catalyzed oxidation of para -alkyl phenols ( p -cresol, 3,4-dimethylphenol, tyrosol, 2′- O -acetyl-tyrosol) in biphasic systems has been investigated. With all the substrates compounds similar to the so-called “Pummerer's ketone” co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0a94be3e9b30089d3ef741134253c07d
https://doi.org/10.1016/j.molcatb.2009.12.016

Enzymatic acylation as an efficient tool for an easy access to specific acyl derivatives of the natural antioxidants verbascoside, teupolioside and echinacoside

Autor: Stefania Caufin, Sergio Riva, Bruno Danieli, Cristina Navarra

Publikováno v: Journal of molecular catalysis. B, Enzymatic (Online) 104 (2014): 42–47. doi:10.1016/j.molcatb.2014.02.019
info:cnr-pdr/source/autori:Caufin S.; Navarra C.; Riva S.; Danieli B./titolo:Enzymatic acylation as an efficient tool for an easy access to specific acyl derivatives of the natural antioxidants verbascoside, teupolioside and echinacoside/doi:10.1016%2Fj.molcatb.2014.02.019/rivista:Journal of molecular catalysis. B, Enzymatic (Online)/anno:2014/pagina_da:42/pagina_a:47/intervallo_pagine:42–47/volume:104

The natural antioxidants phenylpropanoids glycosides echinacoside (1), verbascoside (2) and teupolioside (3) were efficiently and regiospecifically monoacylated by means of the enzyme lipase PS. While acylation of teupolioside (3) and of echinacoside

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9609ef265e51204e6ce64df05c234d4
http://www.cnr.it/prodotto/i/286642