Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Damiano Cancogni"'
Autor:
Laura Morelli, Damiano Cancogni, Marta Tontini, Alberto Nilo, Sara Filippini, Paolo Costantino, Maria Rosaria Romano, Francesco Berti, Roberto Adamo, Luigi Lay
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2367-2376 (2014)
A vaccine to prevent infections from the emerging Neisseria meningitidis X (MenX) is becoming an urgent issue. Recently MenX capsular polysaccharide (CPS) fragments conjugated to CRM197 as carrier protein have been confirmed at preclinical stage as p
Externí odkaz:
https://doaj.org/article/02b161b95d3743a199d770006c294956
Autor:
Matteo Tommasini, Andrea Lucotti, Damiano Cancogni, Francesca Fontana, Paolo Maria Ossi, Sebastiano Trusso, Chiara Zanchi
Publikováno v:
Chirality (N.Y., N.Y. Print) 30 (2018): 875–882. doi:10.1002/chir.22970
info:cnr-pdr/source/autori:Zanchi, Chiara; Lucotti, Andrea; Cancogni, Damiano; Fontana, Francesca; Trusso, Sebastiano; Ossi, Paolo M.; Tommasini, Matteo/titolo:Functionalization of nanostructured gold substrates with chiral chromophores for SERS applications: The case of 5-Aza[5]helicene/doi:10.1002%2Fchir.22970/rivista:Chirality (N.Y., N.Y. Print)/anno:2018/pagina_da:875/pagina_a:882/intervallo_pagine:875–882/volume:30
info:cnr-pdr/source/autori:Zanchi, Chiara; Lucotti, Andrea; Cancogni, Damiano; Fontana, Francesca; Trusso, Sebastiano; Ossi, Paolo M.; Tommasini, Matteo/titolo:Functionalization of nanostructured gold substrates with chiral chromophores for SERS applications: The case of 5-Aza[5]helicene/doi:10.1002%2Fchir.22970/rivista:Chirality (N.Y., N.Y. Print)/anno:2018/pagina_da:875/pagina_a:882/intervallo_pagine:875–882/volume:30
Nanostructured gold thin films can be fabricated by controlled pulsed laser deposition to get efficient sensors, with uniform morphology and optimized plasmon resonance, to be employed as plasmonic substrates in surface enhanced Raman scattering spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90402e2d62fec8027a7d9383442c8304
http://hdl.handle.net/10446/128356
http://hdl.handle.net/10446/128356
Autor:
Luigi Lay, Damiano Cancogni
Publikováno v:
Synlett (Stuttg.) 25 (2014): 000A–000F. doi:10.1055/s-0034-1379471
info:cnr-pdr/source/autori:Cancogni, Damiano; Lay, Luigi/titolo:Exploring glycosylation reactions under continuous-flow conditions/doi:10.1055%2Fs-0034-1379471/rivista:Synlett (Stuttg.)/anno:2014/pagina_da:000A/pagina_a:000F/intervallo_pagine:000A–000F/volume:25
info:cnr-pdr/source/autori:Cancogni, Damiano; Lay, Luigi/titolo:Exploring glycosylation reactions under continuous-flow conditions/doi:10.1055%2Fs-0034-1379471/rivista:Synlett (Stuttg.)/anno:2014/pagina_da:000A/pagina_a:000F/intervallo_pagine:000A–000F/volume:25
The industrial development of carbohydrate-based drugs is greatly thwarted by the typical challenges inherent in oligosaccharide synthesis. The practical advantages of continuous-flow synthesis in microreactors (high reproducibility, easy scalability
Publikováno v:
Polysaccharides ISBN: 9783319037516
Polysaccharides
Polysaccharides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd0ec6fa60346a40ce8a33c2aa4b67f
https://doi.org/10.1007/978-3-319-03751-6_65-1
https://doi.org/10.1007/978-3-319-03751-6_65-1
Publikováno v:
Tetrahedron Letters. 51:5385-5387
The Letter reports a safe and reliable synthesis of aryl 1,2,3-triazoles from the corresponding anilines via intermediate aryl azides, using a continuous process. The method was applied to a variety of substrates with good to excellent yields, withou
Publikováno v:
European journal of organic chemistry
(2012): 1336–1345. doi:10.1002/ejoc.201101320
info:cnr-pdr/source/autori:Cancogni, Damiano; Mandoli, Alessandro; Jumde, Ravindra P.; Pini, Dario/titolo:Silicone-Supported Cinchona Alkaloid Derivatives as Insoluble Organocatalysts in the Enantioselective Dimerization of Ketenes/doi:10.1002%2Fejoc.201101320/rivista:European journal of organic chemistry (Print)/anno:2012/pagina_da:1336/pagina_a:1345/intervallo_pagine:1336–1345/volume
(2012): 1336–1345. doi:10.1002/ejoc.201101320
info:cnr-pdr/source/autori:Cancogni, Damiano; Mandoli, Alessandro; Jumde, Ravindra P.; Pini, Dario/titolo:Silicone-Supported Cinchona Alkaloid Derivatives as Insoluble Organocatalysts in the Enantioselective Dimerization of Ketenes/doi:10.1002%2Fejoc.201101320/rivista:European journal of organic chemistry (Print)/anno:2012/pagina_da:1336/pagina_a:1345/intervallo_pagine:1336–1345/volume
A straightforward procedure is presented for the covalentimmobilization of ester and silyl ether derivatives of theCinchona alkaloid 10,11-dihydroquinidine within insoluble cross-linked silicone elastomeric films. These materials were effective heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::659ad3e34a23efeec1b9b52056ba3ded
Publikováno v:
ChemInform. 42
Autor:
Giorgio Tseberlidis, Paolo Zardi, Alessandro Caselli, Damiano Cancogni, Matteo Fusari, Luigi Lay, Emma Gallo
Publikováno v:
Organometallics; Aug2015, Vol. 34 Issue 15, p3774-3781, 8p