Zobrazeno 1 - 10
of 50
pro vyhledávání: '"van Axel Castelli V."'
Autor:
van Axel castelli, V., van Axel Castelli, Valeria, Dalla Cort, Antonella, Mandolini, Luigi, Pinto, Valentina, Reinhoudt, David, Ribaudo, Fabrizio, Sanna, Cecilia, Schiaffino, Luca, Ruel, Bianca H.M.
Publikováno v:
Supramolecular chemistry, 14(2-3), 211-219. Taylor & Francis
The complexation of the salophen-uranyl metallocleft 2 and of its half-cleft analogue 3 with enones and other carbonyl compounds was assessed in chloroform by UV-Vis titration and, occasionally, by FT-IR measurements. Complexes with receptors 2 and 3
Autor:
Van Axel Castelli, V., Trivieri, G., Zucchelli, I., Brambilla, Luigi, Barbuzzi, T., Castiglioni, Chiara, Paci, M., Zerbi, Giuseppe, Zanol, M.
Publikováno v:
Journal of pharmaceutical sciences. 97(9)
Parenterally administered cladribine (2-chloro-2'-deoxyadenosine) has demonstrated promising efficacy and safety in clinical trials in patients with multiple sclerosis (MS). An oral formulation of this small molecule would be an attractive option for
Autor:
Hetterscheid D.G.H., Hendriksen C., Dzik W.I., SmitsJ.M.M., van EckE.R.H., Rowan A.E., Busico V., Vacatello M., Van Axel Castelli V., Segre A.L., Jellema E., Bloemberg T, G.H., de Bruin B.
Publikováno v:
Journal of the American Chemical Society
128 (2006): 9746–9752.
info:cnr-pdr/source/autori:Hetterscheid D.G.H., Hendriksen C., Dzik W.I., SmitsJ.M.M., van EckE.R.H., Rowan A.E., Busico V., Vacatello M., Van Axel Castelli V., Segre A.L., Jellema E., Bloemberg T,G.H.,de Bruin B./titolo:Rhodium-Mediated Stereoselective Polymerization of/doi:/rivista:Journal of the American Chemical Society (Print)/anno:2006/pagina_da:9746/pagina_a:9752/intervallo_pagine:9746–9752/volume:128
128 (2006): 9746–9752.
info:cnr-pdr/source/autori:Hetterscheid D.G.H., Hendriksen C., Dzik W.I., SmitsJ.M.M., van EckE.R.H., Rowan A.E., Busico V., Vacatello M., Van Axel Castelli V., Segre A.L., Jellema E., Bloemberg T,G.H.,de Bruin B./titolo:Rhodium-Mediated Stereoselective Polymerization of/doi:/rivista:Journal of the American Chemical Society (Print)/anno:2006/pagina_da:9746/pagina_a:9752/intervallo_pagine:9746–9752/volume:128
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::bfe3d3f62337c85a4127134e924b4320
https://publications.cnr.it/doc/33236
https://publications.cnr.it/doc/33236
Autor:
Grigurina I., Mariotti F., Fogliano V., Gallo M., Scaloni A., Iacobellis N.S., Lo Cantore P., Mannina L., Van Axel Castelli V., Greco M.L., Graniti A.
Publikováno v:
1597 (2002): 81–89.
info:cnr-pdr/source/autori:Grigurina I., Mariotti F., Fogliano V., Gallo M., Scaloni A., Iacobellis N.S., Lo Cantore P., Mannina L., Van Axel Castelli V., Greco M.L., Graniti A./titolo:A new syringopeptin produced by bean strains of the Pseudomonas syringae pv. Syringae/doi:/rivista:/anno:2002/pagina_da:81/pagina_a:89/intervallo_pagine:81–89/volume:1597
info:cnr-pdr/source/autori:Grigurina I., Mariotti F., Fogliano V., Gallo M., Scaloni A., Iacobellis N.S., Lo Cantore P., Mannina L., Van Axel Castelli V., Greco M.L., Graniti A./titolo:A new syringopeptin produced by bean strains of the Pseudomonas syringae pv. Syringae/doi:/rivista:/anno:2002/pagina_da:81/pagina_a:89/intervallo_pagine:81–89/volume:1597
Two strains (B728a and Y37) of the phytopathogenic bacterium Pseudomonas syringae pv. syringae isolated from bean (Phaseolus vulgaris) plants were shown to produce in culture both syringomycin, a lipodepsinonapeptide secreted by the majority of the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::95b1fdefcd9a0e52eb86198a9499275b
http://www.cnr.it/prodotto/i/32959
http://www.cnr.it/prodotto/i/32959
Autor:
van Axel Castelli V., Dalla Cort A., Mandolini L., Pinto V., Reinhoudt D. N., Ribaudo F., Sanna C., Schiaffino L., Snellink-Ruel B. H. M.
Publikováno v:
Supramolecular chemistry
14 (2002): 211–219.
info:cnr-pdr/source/autori:van Axel Castelli V., Dalla Cort A., Mandolini L., Pinto V., Reinhoudt D. N., Ribaudo F., Sanna C., Schiaffino L., Snellink-Ruel B. H. M./titolo:Molecular Recognition of Carbonyl Compounds by Salophen-uranyl Based Neutral Receptors Driven by van der Waals Forces/doi:/rivista:Supramolecular chemistry (Print)/anno:2002/pagina_da:211/pagina_a:219/intervallo_pagine:211–219/volume:14
14 (2002): 211–219.
info:cnr-pdr/source/autori:van Axel Castelli V., Dalla Cort A., Mandolini L., Pinto V., Reinhoudt D. N., Ribaudo F., Sanna C., Schiaffino L., Snellink-Ruel B. H. M./titolo:Molecular Recognition of Carbonyl Compounds by Salophen-uranyl Based Neutral Receptors Driven by van der Waals Forces/doi:/rivista:Supramolecular chemistry (Print)/anno:2002/pagina_da:211/pagina_a:219/intervallo_pagine:211–219/volume:14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::49e9cf92f1528a092a25d09f5218dbaa
https://publications.cnr.it/doc/16431
https://publications.cnr.it/doc/16431
Autor:
van Axel castelli, V., van Axel Castelli, Valeria, Dalla Cort, Antonella, Mandolini, Luigi, Reinhoudt, David, Schiaffino, Luca
Publikováno v:
Chemistry : a European journal, 6(7), 1193-1198. Wiley-VCH Verlag
ResearcherID
ResearcherID
The base induced addition of benzenethiol to 2-cyclohexen-1-one and its 4, 4-, 5, 5- and 6,6-dimethyl derivatives is catalysed by a salophen-uranyl based metallocleft 2 in chloroform solution with high turnover efficiency and low product inhibition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cd328825ddb536aa156d40e788f9898
http://hdl.handle.net/11573/362521
http://hdl.handle.net/11573/362521