A ERMILI
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Explore the profile of A ERMILI including associated specialties, affiliations and a list of published articles.
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34
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1
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Recent Articles
1.
Balbi A, Ferreccio R, Mazzei M, ERMILI A, Roma G
Farmaco Sci
. 1986 Dec;
41(12):942-53.
PMID: 3556568
N,N,N',N'-Tetrasubstituted 2-(2-aminophenoxy)malonamides (IX) in the presence of phosphorus oxychloride led to the formation of N,N-dialkyl-3-(dialkylamino)-2H-1,4-benzoxazine-2-carboxamides (XII). In the same way 2-(2-amino-3-pyridyloxy)-N,N,N',N'-tetraethylmalonamide (X) yielded 3-(diethylamino)-N,N-diethyl-2H-pyrido[3,2-b] [1,4]oxazine-2-carboxamide (XIII). Also N,N-dialkyl-2-(2-aminophenoxy)acetamides (XIV) by...
2.
Mazzei M, ERMILI A, Balbi A, Di Braccio M, Schiantarelli P, Cadel S
Farmaco Sci
. 1986 Aug;
41(8):611-21.
PMID: 3743752
Through the reaction of resorcin with N,N-dialkylethoxy-carbonylacetamides in suitable conditions 2-(dialkylamino)-5-hydroxychromones (II) were available. Transformation of these compounds into [5-acetoxy-2-(dialkylamino)-4H-chromen-4-ylidene] malononitriles (VII) by reaction with malononitrile in acetic anhydride and...
3.
Mazzei M, Balbi A, ERMILI A, Sottofattori E, Roma G, Schiantarelli P, et al.
Farmaco Sci
. 1985 Dec;
40(12):895-908.
PMID: 2868920
Since 2-(diethylamino)-7-methoxychromone (III a) showed remarkable activity in the rat PCA test, some modifications to its structure were made. For instance new substituents such as chlorine or nitro group were...
4.
Mazzei M, Balbi A, ERMILI A, Roma G
Farmaco Prat
. 1985 Aug;
40(8):266-72.
PMID: 4029372
No abstract available.
5.
6.
Roma G, Balbi A, ERMILI A, Vigevani E
Farmaco Sci
. 1983 Aug;
38(8):546-58.
PMID: 6137413
The reaction of 4-(dialkylamino)-1,3-dihydro-2H-1,5-benzodiazepin-2-ones (I a-c) with N,N-dimethylformamide in the presence of phosphorus pentachloride at room temperature gave rise to the formation of 4-(dialkylamino)-3-[(dimethylamino)methylene]-1,3-dihydro-2H-1,5-benzodiazepin- 2-ones (IX a-c) which were useful...
7.
Balbi A, Roma G, ERMILI A, Ambrosini A, Passerini N
Farmaco Sci
. 1982 Sep;
37(9):582-96.
PMID: 7128815
Some 2-(dialkylamino)chromones phenyl substituted in position 6 or 7 or 8 were synthesized by reaction of N,N-dialkylethoxycarbonylacetamides with 4- or 3- or 2-biphenylol, respectively, in the presence of phosphorus oxychloride....
8.
Balbi A, Di Braccio M, Roma G, ERMILI A, Ambrosini A, Passerini N
Farmaco Sci
. 1979 Jul;
34(7):595-611.
PMID: 477969
3-Alkyl(phenyl)aminoaphtho[2,1-b]pyran-1-ones (III) were prepared from N-alkyl or N-phenylethoxycarbonylacetamides and 2-naphthol in the presence of phosphorus oxychloride, in order to evaluate their pharmacological activity on the CNS in comparison with previously...
9.
ERMILI A, Roma G, Buonamici M, Cuttica A, Galante M, Orsini G, et al.
Farmaco Sci
. 1979 Jun;
34(6):535-44.
PMID: 467630
A 1H-naphtho[2,1-b]pyran derivative (K 8409) has undergone pharmacological investigation for psychotropic activity. The results show potential antidepressant action quantitatively similar to that of imipramine and amitriptyline, but due rather to...
10.
Mazzei M, Roma G, ERMILI A, Cacciatore C
Farmaco Sci
. 1979 Jun;
34(6):469-77.
PMID: 467627
Treatment of N-alkylanilines or diphenylamine with N,N-dialkylethoxycarbonylacetamides in the presence of phosphorus oxychloride afforded 6-alkyl(phenyl)-4-dialkylaminopyrano [3,2-c] quinoline-2,5-(6H)-diones, two molecules of amide being involved in the reaction. In some instances 6-alkyl(phenyl)-4-alkylaminopyrano...