Filippo M Perna
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Explore the profile of Filippo M Perna including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
128
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Recent Articles
1.
Dilauro G, Luccarelli C, Quivelli A, Vitale P, Perna F, Capriati V
Angew Chem Int Ed Engl
. 2023 May;
62(30):e202304720.
PMID: 37166367
Advancing the development of perfecting the use of polar organometallics in bio-inspired solvents, we report on the effective generation in batch of organosodium compounds, by the oxidative addition of a...
2.
Quivelli A, Marino M, Vitale P, Garcia-Alvarez J, Perna F, Capriati V
ChemSusChem
. 2021 Nov;
15(1):e202102211.
PMID: 34762333
An efficient and novel protocol was developed for a Cu-catalyzed Ullmann-type aryl alkyl ether synthesis by reacting various (hetero)aryl halides (Cl, Br, I) with alcohols as active components of environmentally...
3.
Dilauro G, Azzollini C, Vitale P, Salomone A, Perna F, Capriati V
Angew Chem Int Ed Engl
. 2021 Feb;
60(19):10632-10636.
PMID: 33605516
Pd-catalyzed Negishi cross-coupling reactions between organozinc compounds and (hetero)aryl bromides have been reported when using bulk water as the reaction medium in the presence of NaCl or the biodegradable choline...
4.
Cicco L, Hernandez-Fernandez J, Salomone A, Vitale P, Ramos-Martin M, Gonzalez-Sabin J, et al.
Org Biomol Chem
. 2021 Feb;
19(8):1773-1779.
PMID: 33543179
An efficient and selective N-functionalization of amides is first reported via a CuI-catalyzed Goldberg-type C-N coupling reaction between aryl iodides and primary/secondary amides run either in Deep Eutectic Solvents (DESs)...
5.
Vitale P, Cicco L, Cellamare I, Perna F, Salomone A, Capriati V
Beilstein J Org Chem
. 2020 Aug;
16:1915-1923.
PMID: 32802208
We report that phenacyl azides are key compounds for a regiodivergent synthesis of valuable, functionalized imidazole (32-98% yield) and pyrimidine derivatives (45-88% yield), with a broad substrate scope, when using...
6.
Cicco L, Fombona-Pascual A, Sanchez-Condado A, Carriedo G, Perna F, Capriati V, et al.
ChemSusChem
. 2020 Jul;
13(18):4967-4973.
PMID: 32666628
Highly polarized lithium phosphides (LiPR ) were synthesized, for the first time, in deep eutectic solvents as sustainable reaction media, at room temperature and in the absence of protecting atmosphere,...
7.
Cicco L, Salomone A, Vitale P, Rios-Lombardia N, Gonzalez-Sabin J, Garcia-Alvarez J, et al.
ChemSusChem
. 2020 May;
13(14):3583-3588.
PMID: 32445433
Highly polarized organometallic compounds of s-block elements are added smoothly to chiral N-tert-butanesulfinyl imines in the biodegradable d-sorbitol/choline chloride eutectic mixture, thereby granting access to enantioenriched primary amines after quantitatively...
8.
Piemontese L, Sergio R, Rinaldo F, Brunetti L, Perna F, Santos M, et al.
Molecules
. 2020 Feb;
25(3).
PMID: 32013037
An unsubstituted 2-hydroxyphenylbenzimidazole has recently been included as a scaffold in a series of hybrids (including the hit compound PZ1) based on the framework of the acetylcholinesterase (AChE) inhibitor Donepezil,...
9.
Dilauro G, Garcia S, Tagarelli D, Vitale P, Perna F, Capriati V
ChemSusChem
. 2018 Aug;
11(19):3495-3501.
PMID: 30074303
Pd-catalyzed Suzuki-Miyaura cross-coupling between (hetero)aryl halides (Cl, Br, I) and versatile, moisture-stable mono- and bifunctional potassium aryltrifluoroborates proceeded efficiently and chemoselectively in air and under generally mild conditions; a catalyst...
10.
Cicco L, Sblendorio S, Mansueto R, Perna F, Salomone A, Florio S, et al.
Chem Sci
. 2018 Jun;
7(2):1192-1199.
PMID: 29910874
It has always been a firm conviction of the scientific community that the employment of both anhydrous conditions and water-free reaction media is required for the successful handling of organometallic...