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Autor:
Sergio Riva, Bruno Danieli
Publikováno v:
Current Organic Chemistry. 7:i-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72632ca27f70b3f2d50b22d53328bc94
https://doi.org/10.2174/1385272033486413
https://doi.org/10.2174/1385272033486413
Publikováno v:
Catalysts; Volume 13; Issue 5; Pages: 819
The enzymatic acetylation in the organic solvents of a number of the important bioactive cardiac glycosides was investigated. With the bufanolide proscillaridin A and the cardenolide lanatoside C, acylation, as expected, occurred at the secondary 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b483847a0c4354c8e8b868cf7305b30f
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de450484590f60c13e4d4846747441bc
http://www.scopus.com/inward/record.url?eid=2-s2.0-84978062880&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84978062880&partnerID=MN8TOARS
Autor:
Riva, Sergio, Danieli, Bruno
Publikováno v:
Current Organic Chemistry; September 2003, Vol. 7 Issue: 13 p1-1, 1p
Autor:
Riva, Sergio, Danieli, Bruno
Publikováno v:
Current Organic Chemistry; September 2003, Vol. 7 Issue: 13 pi-i, 1p
Autor:
Sergio Crippa, Bruno Danieli, Giovanna Pressi, Anacleto Minghetti, Fabiana Antognoni, Ferruccio Poli, Roberto Dal Toso, Nicoletta Crespi Perellino
Publikováno v:
Fitoterapia. 82:950-954
3,5-O-dicaffeoyl-4-O-malonilquinic acid (1) (irbic acid) has been isolated for the first time from cell cultures of Centella asiatica and till now it has never been reported to be present in the intact plant. Evidence of its structure was obtained by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b424548cd79c7209367deb7ed8f22f0
https://doi.org/10.1016/j.fitote.2011.05.008
https://doi.org/10.1016/j.fitote.2011.05.008
Autor:
Sergio Riva, Daniela Monti, Bruno Danieli, Stefania Caufin, Paolo Gavezzotti, Pietro Magrone, Cristina Navarra
Publikováno v:
Advanced synthesis & catalysis
353 (2011): 2421–2430. doi:10.1002/adsc.201100413
info:cnr-pdr/source/autori:Gavezzotti, Paolo; Navarra, Cristina; Caufin, Stefania; Danieli, Bruno; Magrone, Pietro; Monti, Daniela; Riva, Sergio/titolo:Synthesis of Enantiomerically Enriched Dimers of Vinylphenols by Tandem Action of Laccases and Lipases/doi:10.1002%2Fadsc.201100413/rivista:Advanced synthesis & catalysis (Print)/anno:2011/pagina_da:2421/pagina_a:2430/intervallo_pagine:2421–2430/volume:353
353 (2011): 2421–2430. doi:10.1002/adsc.201100413
info:cnr-pdr/source/autori:Gavezzotti, Paolo; Navarra, Cristina; Caufin, Stefania; Danieli, Bruno; Magrone, Pietro; Monti, Daniela; Riva, Sergio/titolo:Synthesis of Enantiomerically Enriched Dimers of Vinylphenols by Tandem Action of Laccases and Lipases/doi:10.1002%2Fadsc.201100413/rivista:Advanced synthesis & catalysis (Print)/anno:2011/pagina_da:2421/pagina_a:2430/intervallo_pagine:2421–2430/volume:353
The tandem use of laccases and lipases has been exploited for the simple preparative synthesis of enantiomerically enriched dimeric phenols. Laccase-catalyzed oxidation of isoeugenol (1) and vinylguaiacol (7) in biphasic systems gave as main products
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6fd44e1abd9d3abcf32cc6090b44347
https://doi.org/10.1002/adsc.201100413
https://doi.org/10.1002/adsc.201100413
Autor:
Lasse Evensen, Jürgen Borlak, James B. Lorens, Daniele Passarella, Lisa Dalla Via, Stella Borrelli, Daniela Comi, Bruno Danieli, Ornella Gia, Elena Riva, Gabriele Fontana, Francesco Colombo
Publikováno v:
Bioorganic & Medicinal Chemistry. 18:8660-8668
The preparation and biological evaluation of a novel series of dimeric camptothecin derivatives are described. All the new compounds showed a significant ability to inhibit human tumor cell growth with IC50 values ranging from 0.03 to 12.2 μM. The i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecdae787ddc6ff2fc150037427a122e4
https://doi.org/10.1016/j.bmc.2010.09.069
https://doi.org/10.1016/j.bmc.2010.09.069
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
https://doi.org/10.1016/j.molcatb.2009.12.016