Pregled bibliografske jedinice broj: 242051
Synthesis and Antimicrobial Activity of Some Derivatives on the Basis (7-hydroxy-2-oxo-2H-chromen-4-yl)-acetic Acid Hydrazide
Synthesis and Antimicrobial Activity of Some Derivatives on the Basis (7-hydroxy-2-oxo-2H-chromen-4-yl)-acetic Acid Hydrazide // Molecules, 11 (2006), 1; 134-147 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 242051 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and Antimicrobial Activity of Some Derivatives on the Basis (7-hydroxy-2-oxo-2H-chromen-4-yl)-acetic Acid Hydrazide
Autori
Čačić, Milan ; Trkovnik, Mladen ; Čačić, Frane ; Has-Schön, Elizabeta
Izvornik
Molecules (1420-3049) 11
(2006), 1;
134-147
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
coumarin hydrazide; Schiff's bases; thiosemicarbazide; oxadiazole; triazole
Sažetak
(7-Hydroxy-2-oxo-2H-chromen-4-yl)-acetic acid hydrazide (2) was prepared from (7-hydroxy-2-oxo-2H-chromen-4-yl)-acetic acid ethyl ester (1) and 100% hydrazine hydrate. Compound 2, is the key intermediate for the synthesis of several series of new compounds such as Schiff's bases 3a-l, formic acid N'-[2-(7-hydroxy-2-oxo-2Hchromen- 4-yl)- acetyl]-hydrazide (4), acetic acid N'-[2-(7-hydroxy-2-oxo-2H-chromen-4-yl)-acetyl]-hydrazide (5), (7-hydroxy-2-oxo-2H-chromen-4-yl)-acetic acid N'-[2-(4-hydroxy-2-oxo-2H-chromen-3-yl)-2-oxo-ethyl]-hydrazide (6), 4-phenyl-1-(7-hydroxy-2- oxo-2H-chromen-4-acetyl)-thiosemicarbazide (7), ethyl 3-{;2-[2-(7-hydroxy-2-oxo-2Hchromen- 4-yl)-acetyl]hydrazono};butanoate (8), (7-hydroxy-2-oxo-2H-chromen-4-yl)- acetic acid N'-[(4-trifluoromethyl-phenylimino)-methyl]-hydrazide (9) and (7-hydroxy-2-oxo-2H-chromen-4-yl)-acetic acid N'-[(2, 3, 4-trifluorophenylimino)-methyl]-hydrazide (10). Cyclocondensation of compound 2 with pentane-2, 4-dione gave 4-[2-(3, 5-dimethyl- 1H-pyrazol-1-yl)-2-oxoethyl]-7-hydroxy-2H-chromen-2-one (11), while with carbondisulfide it afforded 7-hydroxy-4-[(5-mercapto-1, 3, 4-oxadiazol-2-yl)methyl]-2Hchromen- 2-one (12) and with potassium isothiocyanate it gave 7-hydroxy-4-[(5- mercapto-4H-1, 2, 4-triazol-3-yl)methyl]-2H-chromen-2-one (14). Compound 7 was cyclized to afford 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)-N´-(4-oxo-2-phenyliminothiazolidin-3-yl)-acetamide (15).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Prehrambeno-tehnološki fakultet, Osijek,
Sveučilište u Osijeku, Odjel za matematiku
Profili:
Frane Čačić Kenjerić
(autor)
Mladen Trkovnik
(autor)
Milan Čačić
(autor)
Elizabeta Has-Schon
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE