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article
chemical structure
proton nuclear magnetic resonance
synthesis
unclassified drug
carbon nuclear magnetic resonance
12
cyclization
6
heterocyclic compound
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reaction analysis
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acetylation
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chemical reaction
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diastereoisomer
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drug conformation
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infrared spectroscopy
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nuclear Overhauser effect
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oxadiazole derivative
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1 aminocarbazole
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1 benzoylcarbazole
2
1 bromocarbazole
2
1 chlorocarbazole
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1 iodocarbazole
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1 nitrocarbazole
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1,4 naphthoquinone derivative
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2 (4 chlorophenyl) 5 [1',2',3',5' penta o benzoyl d galactopentitol 1 yl] 1,3,4 oxadiazole
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2 acetamido 4 n acetyl 3' spiro[1',2':5',6' di o isopropylidene alpha dextro glucofuranosyl] 1,3,4 thiadiazoline
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2 hydroxycarbazole
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2 phenyl 5 [1',2',3',4',5' penta o benzoyl d galactopentitol 1 yl] 1,3,4 oxadiazole
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2 propyl 3,4 dideoxy alpha dextro erythrohex 3 enopyranoside
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2 propyl 6 o acetyl 3,4 anhydro alpha dextro allopyranoside
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2,3,7,8,13,17,18 octabromo 5,10,15,20 tetrakis(pentafluorophenyl)porphyrin
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