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unclassified drug
article
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carbon nuclear magnetic resonance
3
chemical structure
3
heterocyclic compound
3
proton nuclear magnetic resonance
3
acetylation
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oxadiazole derivative
2
tetrazole derivative
2
thiosemicarbazone derivative
2
1,2,3,4 di o isopropylidene beta levo arabinopyranos 5 yl
1
1,3,3 trimethyl 2 norcamphanone
1
2 phenyl 5 glycosyl 1,3,4 oxadiazole
1
3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
1
3,4' dimethoxybenzophenone thiocarbamazone
1
4 methoxybenzophenone thiocarbamazone
1
4,4' dimethoxybenzophenone thiocarbamazone
1
5 [5' (1',2':3',4' di o isopropylidene beta levo arabinopyranosyl]tetrazole
1
5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
1
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
1
5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
1
5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
1
5 methoxyindan 1 one thiosemicarbazone
1
5 methyl 2 [5' (1',2':3',4' di o isoproylidene beta levo arabinosyl] 1,3,4 oxadiazole
1
5 phenyl 2 [5' (1',2':3',4' di o isoproylidene beta levo arabinosyl] 1,3,4 oxadiazole
1
6 methoxyindan 1 one thiosemicarbazone
1
Acylation
1
Aromatic compounds
1
Asymmetric spiro-heterocyclic compounds
1
Butanes
1
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1
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2por Martins Alho, Miriam Amelia, Moltrasio, Graciela Yolanda, D'Accorso, Norma Beatriz
Publicado 2002 -
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