Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Valentina Gandolfo"'
Autor:
Eleonora Barone, Giovanna Ponticello, Pieramaria Giaramida, Margherita Squadrito, Teresa Fasciana, Valentina Gandolfo, Francesco Ardizzone, Manuela Monteleone, Onofrio Corona, Nicola Francesca, Daniele Oliva
Publikováno v:
Fermentation, Vol 7, Iss 2, p 79 (2021)
An increasing interest in novel wine productions is focused on non-Saccharomyces yeasts due to their potential in improving sensory profiles. Although Kluyveromyces marxianus has been originally isolated from grapes and its enzymatic activities are u
Externí odkaz:
https://doaj.org/article/b1a8b63d293742a4b5981c9fd8e3bd11
Autor:
Giovanna Ponticello, M Squadrito, Francesco Ardizzone, Manuela Monteleone, Daniele Oliva, Valentina Gandolfo, Teresa Fasciana, Onofrio Corona, Eleonora Barone, Pieramaria Giaramida, Nicola Francesca
Publikováno v:
Fermentation, Vol 7, Iss 79, p 79 (2021)
Fermentation
Volume 7
Issue 2
Fermentation
Volume 7
Issue 2
An increasing interest in novel wine productions is focused on non-Saccharomyces yeasts due to their potential in improving sensory profiles. Although Kluyveromyces marxianus has been originally isolated from grapes and its enzymatic activities are u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32d88ab498435b035cad7f4179c3819
http://hdl.handle.net/10447/513179
http://hdl.handle.net/10447/513179
Publikováno v:
European Journal of Organic Chemistry. 2010:2768-2787
Full details of our synthetic approaches directed towards the enantioselective synthesis of new dynemicin analogues each containing a side-arm (a “handle”) incorporating a protected alcohol are reported.
Autor:
Andrea Basso, Monica Paravidino, Giuseppe Giannini, Loana Musso, Luca Banfi, Valentina Gandolfo, Giuseppe Guanti, Renata Riva, Elisabetta Bevilacqua
Lactenediynes are compounds characterized by the fusion of a β-lactam with a cyclodeca-3-ene-1,5-diyne. In this work the most promising members of this family have been activated by attaching a carbalkoxy or a carbamoyl group to the azetidinone nitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b79b221d5ffb914c95377ac5ed8c3d
http://hdl.handle.net/11567/222289
http://hdl.handle.net/11567/222289
Publikováno v:
ChemInform. 35
The new simplified dynemicin analogue 16 was prepared enantio- and diastereoselectively in 17 steps starting from monoacetate (S) 7 . It is equipped with a side arm containing a protected primary alcoholic function (`handle'), which can be used for c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4102f015b1f7941fd638543cc32a00f
http://hdl.handle.net/11567/246025
http://hdl.handle.net/11567/246025