Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Iole Cerminara"'
Autor:
Jessica Bais, Fabio Benedetti, Federico Berti, Iole Cerminara, Sara Drioli, Maria Funicello, Giorgia Regini, Mattia Vidali, Fulvia Felluga
Publikováno v:
Molecules, Vol 25, Iss 18, p 4152 (2020)
A library of dihydropyrimidinones was synthesized via a “one-pot” three component Biginelli reaction using different aldehydes in combination with β-dicarbonyl compounds and urea. Selected 2-thiooxo and 2-imino analogs were also obtained with th
Externí odkaz:
https://doaj.org/article/5f43fc193c9c4cd89b8d7d919e79250c
Publikováno v:
Pharmaceuticals, Vol 5, Iss 3, Pp 297-316 (2012)
This minireview provides a brief outline of the peculiar aspects of the preparation of peptidomimetic and pseudopeptidic structures containing heterocycles. In particular novel tricyclic structures are investigated as potential drugs.
Externí odkaz:
https://doaj.org/article/64f22e83693344319ef6f0596ee1bc7b
Autor:
Federico Berti, Iole Cerminara, Fulvia Felluga, Paolo Lupattelli, Lucia Chiummiento, Maria Funicello
Multicomponent reactions (MCRs) represent very interesting tools to reach eco-friendly and sustainable transformations in organic chemistry. In particular, the Biginelli reaction furnishes a very easy approach to the synthesis of a library of biologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04de22d39343a27024dc28ce40e226ed
http://hdl.handle.net/11573/1653054
http://hdl.handle.net/11573/1653054
Autor:
Iole Cerminara, Jessica Bais, Giorgia Regini, Federico Berti, Sara Drioli, Fabio Benedetti, Maria Funicello, Mattia Vidali, Fulvia Felluga
Publikováno v:
Molecules
Volume 25
Issue 18
Molecules, Vol 25, Iss 4152, p 4152 (2020)
Volume 25
Issue 18
Molecules, Vol 25, Iss 4152, p 4152 (2020)
A library of dihydropyrimidinones was synthesized via a &ldquo
one-pot&rdquo
three component Biginelli reaction using different aldehydes in combination with &beta
dicarbonyl compounds and urea. Selected 2-thiooxo and 2-imino analogs w
one-pot&rdquo
three component Biginelli reaction using different aldehydes in combination with &beta
dicarbonyl compounds and urea. Selected 2-thiooxo and 2-imino analogs w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::492e3326b7efdf4419fdc0f70a41e0aa
Autor:
Francesco Scorza, Paolo Lupattelli, Patrizia Scafato, Maria Funicello, Lucia Chiummiento, Stefano Superchi, Iole Cerminara
Publikováno v:
Computational Science and Its Applications – ICCSA 2020 ISBN: 9783030588199
ICCSA (7)
ICCSA (7)
Green Chemistry, Circular Economy and Sustainability are issues at the center of the modern scientific debate and three major trends in the global market. These three subjects are interconnected and interdependent and represent an affordable set of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78480d1883f9375ac2e859d1c66476db
https://doi.org/10.1007/978-3-030-58820-5_16
https://doi.org/10.1007/978-3-030-58820-5_16
Publikováno v:
Helvetica chimica acta 99 (2016): 384–392. doi:10.1002/hlca.201500285
info:cnr-pdr/source/autori:Cerminara I.; D'Alessio L.; D'auria M.; Funicello M.; Guarnaccio A./titolo:5-Substituted Benzothiophenes: Synthesis, Mechanism, and Kinetic Studies/doi:10.1002%2Fhlca.201500285/rivista:Helvetica chimica acta/anno:2016/pagina_da:384/pagina_a:392/intervallo_pagine:384–392/volume:99
info:cnr-pdr/source/autori:Cerminara I.; D'Alessio L.; D'auria M.; Funicello M.; Guarnaccio A./titolo:5-Substituted Benzothiophenes: Synthesis, Mechanism, and Kinetic Studies/doi:10.1002%2Fhlca.201500285/rivista:Helvetica chimica acta/anno:2016/pagina_da:384/pagina_a:392/intervallo_pagine:384–392/volume:99
The kinetics of the reaction of 4-methoxythiophenoxyacetaldehyde diethyl acetal, 4-nitrothiophenoxyacetaldehyde diethyl acetal, and 3-methoxythiophenoxyacetaldehyde diethyl acetal in polyphosphoric acid has been explained. The kinetic behavior has be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086e8047f3d1d420e83196bf80a794c2
https://doi.org/10.1002/hlca.201500285
https://doi.org/10.1002/hlca.201500285
metodologia per la sintesi di derivati delle benzotieno[2, 3-b]piridine e dmiostrazione della loro attività come inibitori della ß-secretasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::271ad92b043f22e315ec059614530999
https://hdl.handle.net/11368/2848522
https://hdl.handle.net/11368/2848522
Publikováno v:
Medicinal chemistry. 6
4- and 5-substituted benzothiophenes were synthesized as starting scaffold in the construction of benzothieno[b] pyridines. Such structures were designed as potential new inhibitors of BACE 1. Preliminary promising biological data were reported. Thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebb1f78355281b4435513b3993c5ad38
https://doi.org/10.4172/2161-0444.1000373
https://doi.org/10.4172/2161-0444.1000373
Publikováno v:
Pharmaceuticals, Vol 5, Iss 3, Pp 297-316 (2012)
Pharmaceuticals
Pharmaceuticals
This minireview provides a brief outline of the peculiar aspects of the preparation of peptidomimetic and pseudopeptidic structures containing heterocycles. In particular novel tricyclic structures are investigated as potential drugs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c271187f8c7597e1474323303af28186
http://hdl.handle.net/11573/1653044
http://hdl.handle.net/11573/1653044