Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Francesco G. Gatti"'
Autor:
Michele Crotti, Fabio Parmeggiani, Erica Elisa Ferrandi, Francesco G. Gatti, Alessandro Sacchetti, Sergio Riva, Elisabetta Brenna, Daniela Monti
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 7 (2019)
Ene reductases from the Old Yellow Enzyme (OYE) family are industrially interesting enzymes for the biocatalytic asymmetric reduction of alkenes. To access both enantiomers of the target reduced products, stereocomplementary pairs of OYE enzymes are
Externí odkaz:
https://doaj.org/article/ca9d1cb7d59445678eb55e6236f26ce6
Autor:
Elisabetta Brenna, Danilo Colombo, Giuseppe Di Lecce, Francesco G. Gatti, Maria Chiara Ghezzi, Francesca Tentori, Davide Tessaro, Mariacristina Viola
Publikováno v:
Molecules, Vol 25, Iss 8, p 1882 (2020)
A chemo-enzymatic approach for the conversion of oleic acid into azelaic and pelargonic acid is herein described. It represents a sustainable alternative to ozonolysis, currently employed at the industrial scale to perform the reaction. Azelaic acid
Externí odkaz:
https://doaj.org/article/359c26e9e6844ad0aadd3a531da7dcb2
Autor:
Marco G. Rigamonti, Francesco G. Gatti
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 2117-2124 (2015)
The first stereoselective synthesis of lippidulcines A, B and C has been accomplished starting from (+)-hernandulcin, which has been prepared on a multigram scale. The previously assigned absolute configurations have been confirmed. The key steps of
Externí odkaz:
https://doaj.org/article/003760168fd04550b10dd7ac3df8df78
Autor:
Elisabetta Brenna, Michele Crotti, Francesco G. Gatti, Daniela Monti, Fabio Parmeggiani, Andrea Pugliese
Publikováno v:
Molecules, Vol 22, Iss 10, p 1591 (2017)
The use of pheromones in the integrated pest management of insects is currently considered a sustainable and environmentally benign alternative to hazardous insecticides. 4-Methylheptan-3-ol is an interesting example of an insect pheromone, because i
Externí odkaz:
https://doaj.org/article/54b0116206ba44e386568c2b056e8a5a
Autor:
Chiara Allegretti, Paola D'Arrigo, Francesco G. Gatti, Letizia A. M. Rossato, Eleonora Ruffini
Our method for the assessment of the stoichiometric coefficients of trimethylglycine betaine/diol based DESs, by automated measures of 1H-NMR T1, compares well with other analytical techniques.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e2b56abf188c8dfb4a0a55b660265c
https://hdl.handle.net/11311/1228003
https://hdl.handle.net/11311/1228003
Exploitation of Soybean Oil Acid Degumming Waste: Biocatalytic Synthesis of High Value Phospholipids
Autor:
Letizia A. M. Rossato, Andrea Bono, Stefano Serra, Paola D'Arrigo, Francesco G. Gatti, Stefano Marzorati, Alberto Strini, Chiara Allegretti, Davide Tessaro
Publikováno v:
ChemistrySelect 6 (2021): 9157–9163. doi:10.1002/slct.202102191
info:cnr-pdr/source/autori:Chiara Allegretti, Andrea Bono, Paola D'Arrigo, Francesco G. Gatti, Stefano Marzorati, Letizia A. M. Rossato, Stefano Serra, Alberto Strini, Davide Tessaro/titolo:Exploitation of Soybean Oil Acid Degumming Waste: Biocatalytic Synthesis of High Value Phospholipids/doi:10.1002%2Fslct.202102191/rivista:ChemistrySelect/anno:2021/pagina_da:9157/pagina_a:9163/intervallo_pagine:9157–9163/volume:6
info:cnr-pdr/source/autori:Chiara Allegretti, Andrea Bono, Paola D'Arrigo, Francesco G. Gatti, Stefano Marzorati, Letizia A. M. Rossato, Stefano Serra, Alberto Strini, Davide Tessaro/titolo:Exploitation of Soybean Oil Acid Degumming Waste: Biocatalytic Synthesis of High Value Phospholipids/doi:10.1002%2Fslct.202102191/rivista:ChemistrySelect/anno:2021/pagina_da:9157/pagina_a:9163/intervallo_pagine:9157–9163/volume:6
The acid degumming waste of the seeds oil refining industry is currently disposed of, but, instead, it could be exploited as an important source for the preparation of many products. In this work, the waste coming from the soybean oil refining step w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0cde47c3f2a0c4a92cf4c5d2673653f
https://doi.org/10.1002/slct.202102191
https://doi.org/10.1002/slct.202102191
Autor:
Gianluca Accorsi, Guy J. Clarkson, Silvia Venturi, M. Ángeles Farrán, Rosa M. Claramunt, Francesco G. Gatti, Agostina Lina Capodilupo, Salvador Leon Cabanillas
Publikováno v:
New Journal of Chemistry. 45:12471-12478
Photoisomerization of trifluoroacetylated diaryl hydrazones induces a change in color due to the formation of a new hydrogen bond in solution and in the solid state.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c56d06ec13f02b52c1ea84fc1af03c9e
https://doi.org/10.1039/d1nj01677f
https://doi.org/10.1039/d1nj01677f
Autor:
Francesco G. Gatti, Maria Chiara Ghezzi, Chiara Ferrari, Elisabetta Brenna, Francesca Tentori, Fabio Parmeggiani
Publikováno v:
Reaction Chemistry & Engineering. 6:1591-1600
Piperonal is a key ingredient in the flavour and fragrance industry and a useful intermediate for the synthesis of fine chemicals. It is currently prepared by either ozonolysis or chromic acid oxidation of isosafrole, obtained upon isomerization of n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69db75635637bdfaf470b1d22a31cc4f
https://doi.org/10.1039/d1re00173f
https://doi.org/10.1039/d1re00173f
Autor:
Silvia Venturi, Milos Trajkovic, Danilo Colombo, Elisabetta Brenna, Marco W. Fraaije, Francesco G. Gatti, Piero Macchi, Emilio Zamboni
Publikováno v:
The Journal of Organic Chemistry, 87(9), 6499-6503. AMER CHEMICAL SOC INC
We describe the asymmetric synthesis of the most pleasant enantiomer of Jessemal fragrance. The key steps are (i) the one-pot reduction of an α-chloro-tetrasubstituted cyclohexenone to give the chlorohydrin, catalyzed by two stereoselective redox en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e34e0c9ae391b74ac7cedc22a7fd93de
https://research.rug.nl/en/publications/7cf1ba6e-c217-4ea2-abd5-cc0fa0a632e4
https://research.rug.nl/en/publications/7cf1ba6e-c217-4ea2-abd5-cc0fa0a632e4
Autor:
Elisabetta Brenna, Emilio Zamboni, Silvia Venturi, Francesco G. Gatti, Marco W. Fraaije, Piero Macchi, Daniela Monti, Milos Trajkovic, Danilo Colombo
Publikováno v:
ACS catalysis (2020): 13050–13057. doi:10.1021/acscatal.0c04097
info:cnr-pdr/source/autori:Venturi S.; Brenna E.; Colombo D.; Fraaije M.W.; Gatti F.G.; Macchi P.; Monti D.; Trajkovic M.; Zamboni E./titolo:Multienzymatic stereoselective reduction of tetrasubstituted cyclic enones to halohydrins with three contiguous stereogenic centers/doi:10.1021%2Facscatal.0c04097/rivista:ACS catalysis/anno:2020/pagina_da:13050/pagina_a:13057/intervallo_pagine:13050–13057/volume
ACS Catalysis, 10(21), 13050-13057. AMER CHEMICAL SOC
info:cnr-pdr/source/autori:Venturi S.; Brenna E.; Colombo D.; Fraaije M.W.; Gatti F.G.; Macchi P.; Monti D.; Trajkovic M.; Zamboni E./titolo:Multienzymatic stereoselective reduction of tetrasubstituted cyclic enones to halohydrins with three contiguous stereogenic centers/doi:10.1021%2Facscatal.0c04097/rivista:ACS catalysis/anno:2020/pagina_da:13050/pagina_a:13057/intervallo_pagine:13050–13057/volume
ACS Catalysis, 10(21), 13050-13057. AMER CHEMICAL SOC
The asymmetric hydrogenation of conjugated tetrasubstituted alkenes with transition-metal catalysts is a challenging reaction, especially for substrates bearing a halide substituent. We describe a two-step multienzymatic reduction of a series of α-h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85a389de6c61ec0afc5a2d6f98017800
https://doi.org/10.1021/acscatal.0c04097
https://doi.org/10.1021/acscatal.0c04097