Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Alfredo Paio"'
Autor:
Bruna DalPizol Novello, Marcela Maria Zanatta, Felipe Pompolim Mendes, Alfredo Paiola Albrecht, Arthur Arrobas Martins Barroso
Publikováno v:
Acta Scientiarum: Biological Sciences, Vol 45, Iss 1 (2023)
The objective of this review is to bring information about innovations and technologies that, through genetic improvement, are being used to improve the sustainability and productivity of agricultural crops, improve human nutrition, as well as conser
Externí odkaz:
https://doaj.org/article/c8d7396ceebb4e9ea02b251293641c68
Autor:
Annunziata D’Ercole, Lorenzo Pacini, Giuseppina Sabatino, Matteo Zini, Lorenzo Milli, Francesca Nuti, Arianna Ribecai, Alfredo Paio, Paolo Rovero, Anna Maria Papini
Publikováno v:
Organic Process Research & Development. 26:2540-2540
Autor:
Paolo Rovero, Alfredo Paio, Annunziata D’Ercole, Matteo Zini, Francesca Nuti, L. Pacini, Anna Maria Papini, Arianna Ribecai, Giuseppina Sabatino
Publikováno v:
Organic process research & development 25 (2021): 2754–2771. doi:10.1021/acs.oprd.1c00368
info:cnr-pdr/source/autori:D'Ercole, Annunziata; Pacini, Lorenzo; Sabatino, Giuseppina; Zini, Matteo; Nuti, Francesca; Ribecai, Arianna; Paio, Alfredo; Rovero, Paolo; Papini, Anna Maria/titolo:An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer/doi:10.1021%2Facs.oprd.1c00368/rivista:Organic process research & development/anno:2021/pagina_da:2754/pagina_a:2771/intervallo_pagine:2754–2771/volume:25
info:cnr-pdr/source/autori:D'Ercole, Annunziata; Pacini, Lorenzo; Sabatino, Giuseppina; Zini, Matteo; Nuti, Francesca; Ribecai, Arianna; Paio, Alfredo; Rovero, Paolo; Papini, Anna Maria/titolo:An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer/doi:10.1021%2Facs.oprd.1c00368/rivista:Organic process research & development/anno:2021/pagina_da:2754/pagina_a:2771/intervallo_pagine:2754–2771/volume:25
A growing industrial interest toward the peptide drug market fueled the need for the development of effective and cGMP compliant manufacturing methods for these complex molecules. Solid-phase strategies are considered methods of election for medium-l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d29c2a766b49246c4ffd343dfd85a016
https://publications.cnr.it/doc/464122
https://publications.cnr.it/doc/464122
Autor:
L. Pacini, Annunziata D’Ercole, Matteo Zini, Alfredo Paio, Paolo Rovero, Anna Maria Papini, Giuseppina Sabatino, Arianna Ribecai
Publikováno v:
Organic process research & development (2021). doi:10.1021/acs.oprd.0c00490
info:cnr-pdr/source/autori:Papini, Anna Maria; Sabatino, Giuseppina; D'Ercole, Annunziata; Pacini, Lorenzo; Zini, Matteo; Ribecai, Arianna; Paio, Alfredo; Rovero, Paolo/titolo:An optimized scalable fully automated solid-phase microwave-assisted cGMP-ready process for the preparation of eptifibatide/doi:10.1021%2Facs.oprd.0c00490/rivista:Organic process research & development/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Papini, Anna Maria; Sabatino, Giuseppina; D'Ercole, Annunziata; Pacini, Lorenzo; Zini, Matteo; Ribecai, Arianna; Paio, Alfredo; Rovero, Paolo/titolo:An optimized scalable fully automated solid-phase microwave-assisted cGMP-ready process for the preparation of eptifibatide/doi:10.1021%2Facs.oprd.0c00490/rivista:Organic process research & development/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume
We investigated several strategies, based on the use of microwave-assisted solid-phase peptide synthesis (MW-SPPS) and scalable to kilogram-scale manufacturing, for the preparation of Eptifibatide, a disulfide-bridged cyclo-heptapeptide drug approved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87c4b0fe2aba17e3983bfb82d507cdb0
http://hdl.handle.net/2158/1219739
http://hdl.handle.net/2158/1219739
Autor:
Daniele Donati, Stefano Biondi, Alfredo Paio, Stjepan Mutak, Sergio Lociuro, Elisa Piga, Francesca Cardullo, Dražen Pavlović, Daniele Andreotti
Publikováno v:
ACS Medicinal Chemistry Letters. 5:1133-1137
An efficient synthesis of α-amino-γ-lactone ketolide (3) was developed, which provided a versatile intermediate for the incorporation of a variety of aryl and heteroaryl groups onto the C-21 position of clarithromycin via HBTU-mediated amidation. T
Autor:
Daniele Donati, Francesca Cardullo, Carmela Napolitano, Stefano Manfredini, Alfredo Paio, Manuela Borriello
Publikováno v:
Synthetic Communications. 41:2031-2035
A rapid and efficient synthesis of 1-benzyl-2-difluoromethyl-piperazine is herein described. The new pathway has the advantage of avoiding orthogonal protection at the two piperazine nitrogen atoms; therefore it is suitable for access to several 1-be
Autor:
Daniele Andreotti, Roberto Profeta, Alfredo Paio, Simone Spada, Francesco Ferroni, Jens Klein
Publikováno v:
Tetrahedron Letters. 51:5521-5524
Stereochemical and synthetic aspects encountered during the preparation of the four possible isomers of 1 are reported. The 5-aryl 2-azabicyclo [3.2.1] octane derivatives represent a novel class of compounds which can be deemed as an example of aryl-
Autor:
Daniele Donati, Manuela Borriello, Carmela Napolitano, Francesca Cardullo, Alfredo Paio, Stefano Manfredini
Publikováno v:
Tetrahedron. 66:5492-5497
A full study on the synthesis of 3-azabicyclo[4.1.0]heptane-1-carboxylic acid is described. Three different approaches were investigated in order to achieve an efficient synthesis of this unnatural aminoacid. The optimized synthetic route relies upon
Autor:
Giovanna Zinzalla, Carla Marchioro, Laura Casiraghi, Stefano Maiorana, Clara Baldoli, Elisabetta de Magistris, Pierfausto Seneci, and Alfredo Paio, Emanuela Licandro
Publikováno v:
Journal of Combinatorial Chemistry. 5:809-813
Different arene Cr(CO)(3) complexes were supported on a polystyrene isonitrile resin by photochemical-promoted replacement of a chromium carbonyl ligand by the NC group. The supported complexes proved to be stable and were successfully used for furth
Publikováno v:
Tetrahedron letters 44 (2003): 1867–1870. doi:10.1016/S0040-4039(03)00090-X
info:cnr-pdr/source/autori:Paio, Alfredo; Gehanne, Sylvie; Grandini, Elena; Reginato, Gianna; Seneci, Pierfausto/titolo:A new analytical method for anchoring quantification of amines on resin support/doi:10.1016%2FS0040-4039(03)00090-X/rivista:Tetrahedron letters/anno:2003/pagina_da:1867/pagina_a:1870/intervallo_pagine:1867–1870/volume:44
info:cnr-pdr/source/autori:Paio, Alfredo; Gehanne, Sylvie; Grandini, Elena; Reginato, Gianna; Seneci, Pierfausto/titolo:A new analytical method for anchoring quantification of amines on resin support/doi:10.1016%2FS0040-4039(03)00090-X/rivista:Tetrahedron letters/anno:2003/pagina_da:1867/pagina_a:1870/intervallo_pagine:1867–1870/volume:44
A rapid and quantitative method for monitoring the efficiency of coupling of amino compounds to polystyrene resin through a carbamate linker has been developed. para-Nitrophenyl carbonate activating group has been shown to release a valuable chromoph