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chemical structure
article
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unclassified drug
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proton nuclear magnetic resonance
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synthesis
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carbon nuclear magnetic resonance
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heterocyclic compound
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mass spectrometry
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chemical reaction
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oxadiazole derivative
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thiadiazole derivative
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thiosemicarbazone derivative
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3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
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3,4' dimethoxybenzophenone thiocarbamazone
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4 methoxybenzophenone thiocarbamazone
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4,4' dimethoxybenzophenone thiocarbamazone
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5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
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5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
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5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
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5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
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5 methoxyindan 1 one thiosemicarbazone
2
6 methoxyindan 1 one thiosemicarbazone
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anthrone thiosemicarbazone
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antifungal agent
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antiinfective agent
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conference paper
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cyclization
2
drug synthesis
2
hydrogen
2
indan 1 one thiosemicarbazone
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1por Martins Alho, M.A., Moglioni, A.G., Brousse, B., Moltrasio, G.Y., D'Accorso, N.B.
Publicado 2000Artículo publishedVersion -
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10JOUR