1998
DOI: 10.1016/s0014-827x(98)00049-4
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Synthesis, structure elucidation and antimicrobial activity of some 3-hydroxy-2-naphthoic acid hydrazide derivatives

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Cited by 66 publications
(38 citation statements)
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“…N 1 , N 2 and N 4 protones which prove the presence of thiosemicarbazides were detected in 1 H-NMR spectrum (Fig 3) and the information given is supported by the literature. (17)(18)(19)(20)(21)(22). 4c, 4e, 4f, 4h), it was determined that these compounds undergo thione-thiol tautomerism (Fig 4).…”
Section: Synthesis Of Tolmetin Thiosemicarbazidesmentioning
confidence: 99%
“…N 1 , N 2 and N 4 protones which prove the presence of thiosemicarbazides were detected in 1 H-NMR spectrum (Fig 3) and the information given is supported by the literature. (17)(18)(19)(20)(21)(22). 4c, 4e, 4f, 4h), it was determined that these compounds undergo thione-thiol tautomerism (Fig 4).…”
Section: Synthesis Of Tolmetin Thiosemicarbazidesmentioning
confidence: 99%
“…Their anticonvulsant activity were investigated against pentylenetetrazole (PTZ) induced convulsions in mice by Doğan and co-workers (95).…”
Section: Biological Activitymentioning
confidence: 99%
“…Substituted 1,4-Dihydro-3-(3-hydroxy-2-naphthyl)-5H-1,2,4-triazoline-5-thiones 41 18,74 were obtained by the cyclization of thiosemicarbazides 40 in sodium hydroxide solution followed by treatment of the reaction mixture with dil. HCl at 0°C (Scheme 14).…”
Section: Figurementioning
confidence: 99%