Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Adriano Carpita"'
Autor:
Graziano Fusini, Fabio Rizzo, Gaetano Angelici, Emanuela Pitzalis, Claudio Evangelisti, Adriano Carpita
Publikováno v:
Catalysts, Vol 10, Iss 3, p 330 (2020)
Palladium nanoparticles (Pd NPs) synthesized by the metal vapor synthesis technique were supported on poly(4-vinylpyridine) 2% cross-linked with divinylbenzene (Pd/PVPy). Transmission electron microscopy revealed the presence of small metal nanoparti
Externí odkaz:
https://doaj.org/article/be81da5c75f34631adcd1c69558895a2
Autor:
Gianluca Casotti, Graziano Fusini, Claudio Evangelisti, Matteo Ferreri, Luca Pardini, Adriano Carpita, Gaetano Angelici
Publikováno v:
Synthesis (Stuttg.) 52 (2020): 1795–1803. doi:10.1055/s-0039-1690852
info:cnr-pdr/source/autori:Casotti G.; Fusini G.; Ferreri M.; Pardini L.F.; Evangelisti C.; Angelici G.; Carpita A./titolo:Total Synthesis of Asparenydiol by Two Sonogashira Cross-Coupling Reactions Promoted by Supported Pd and Cu Catalysts/doi:10.1055%2Fs-0039-1690852/rivista:Synthesis (Stuttg.)/anno:2020/pagina_da:1795/pagina_a:1803/intervallo_pagine:1795–1803/volume:52
info:cnr-pdr/source/autori:Casotti G.; Fusini G.; Ferreri M.; Pardini L.F.; Evangelisti C.; Angelici G.; Carpita A./titolo:Total Synthesis of Asparenydiol by Two Sonogashira Cross-Coupling Reactions Promoted by Supported Pd and Cu Catalysts/doi:10.1055%2Fs-0039-1690852/rivista:Synthesis (Stuttg.)/anno:2020/pagina_da:1795/pagina_a:1803/intervallo_pagine:1795–1803/volume:52
Asparenydiol, which is an important natural compound with potential pharmacological activities, was synthesized through two Sonogashira cross-coupling reactions catalyzed by supported Pd and Cu catalysts and by a Mitsunobu etherification. The optim
Autor:
Gianluca Casotti, Gabriele Laudadio, Gaetano Angelici, Adriano Carpita, Graziano Fusini, Claudio Evangelisti
Publikováno v:
Journal of Flow Chemistry, 9(2), 133-143. Akademiai Kiadó
Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The
Publikováno v:
European Journal of Organic Chemistry. 2019:1021-1026
Autor:
Adriano Carpita, Fabio Rizzo, Gaetano Angelici, Emanuela Pitzalis, Graziano Fusini, Claudio Evangelisti
Publikováno v:
Catalysts
Volume 10
Issue 3
Catalysts, Vol 10, Iss 3, p 330 (2020)
Catalysts 10 (2020). doi:10.3390/catal10030330
info:cnr-pdr/source/autori:Fusini G.; Rizzo F.; Angelici G.; Pitzalis E.; Evangelisti C.; Carpita A./titolo:Polyvinylpyridine-supported palladium nanoparticles: An efficient catalyst for Suzuki-Miyaura coupling reactions/doi:10.3390%2Fcatal10030330/rivista:Catalysts/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:10
Volume 10
Issue 3
Catalysts, Vol 10, Iss 3, p 330 (2020)
Catalysts 10 (2020). doi:10.3390/catal10030330
info:cnr-pdr/source/autori:Fusini G.; Rizzo F.; Angelici G.; Pitzalis E.; Evangelisti C.; Carpita A./titolo:Polyvinylpyridine-supported palladium nanoparticles: An efficient catalyst for Suzuki-Miyaura coupling reactions/doi:10.3390%2Fcatal10030330/rivista:Catalysts/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:10
Palladium nanoparticles (Pd NPs) synthesized by the metal vapor synthesis technique were supported on poly(4-vinylpyridine) 2% cross-linked with divinylbenzene (Pd/PVPy). Transmission electron microscopy revealed the presence of small metal nanoparti
Autor:
Giovanni Benelli, Andrea Lucchi, Gianluca Casotti, Davide Barsanti, Graziano Fusini, Angelo Canale, Gaetano Angelici, Adriano Carpita
In the present study, eleven new sex-specific components extracted from female rectal gland of olive fruit flies were synthesized and identified. The quantitative determination of those components by GC and GC/EI-MS, at different moments of the insec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c3f876c2cbbad1b589c1a3a0b269c5e
http://hdl.handle.net/11568/925679
http://hdl.handle.net/11568/925679
Autor:
Rinaldo Psaro, Adriano Carpita, Maurizio Benfatto, Graziano Fusini, Antonella Balerna, Claudio Evangelisti
Publikováno v:
ChemPhysChem (Internet) (2017). doi:10.1002/cphc.201700215
info:cnr-pdr/source/autori:Evangelisti, Claudio; Balerna, Antonella; Psaro, Rinaldo; Fusini, Graziano; Carpita, Adriano; Benfatto, Maurizio/titolo:Characterization of a Poly-4-vinylpyridine-Supported CuPd Bimetallic Catalyst for Sonogashira Coupling Reactions./doi:10.1002%2Fcphc.201700215/rivista:ChemPhysChem (Internet)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Evangelisti, Claudio; Balerna, Antonella; Psaro, Rinaldo; Fusini, Graziano; Carpita, Adriano; Benfatto, Maurizio/titolo:Characterization of a Poly-4-vinylpyridine-Supported CuPd Bimetallic Catalyst for Sonogashira Coupling Reactions./doi:10.1002%2Fcphc.201700215/rivista:ChemPhysChem (Internet)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume
CuPd bimetallic Solvated Metal Atoms (SMA) synthesized by metal vapor synthesis (MVS) technique and supported on poly-4-vinylpyridine (PVPy) resin, showed signicantly higher catalytic activity in Sonogashira-type carbon-carbon coupling reactions than
Publikováno v:
Journal of Pest Science. 87:449-457
The braconid parasitoid Psyttalia concolor foraging for larvae of Bactrocera oleae (Diptera: Tephritidae) uses olfactory cues from the larval microhabitat. However, it could rely on the sex pheromones of adults of its host, since B. oleae mating leks
Autor:
Alfio Raspi, Santosh Revadi, Giulia Giunti, Adriano Carpita, Gianfranco Anfora, Giovanni Benelli, Angelo Canale
Publikováno v:
Biological Control. 64:116-124
Psyttalia concolor (Szepligeti) is a koinobiont larval-pupal endoparasitoid of many Tephritidae of great economic importance, such as the medfly, Ceratitis capitata (Wiedemann). In several species of parasitoids it has been demonstrated that the mate
Autor:
Adriano Carpita, Arianna Ribecai
Publikováno v:
Tetrahedron Letters. 50:6877-6881
An unprecedented green methodology is described for the preparation of differently substituted indoles via microwave-assisted cycloisomerization of 2-alkynylaniline derivatives in water. Moderate to good yields in the cyclization can be achieved for