3,5-Dimethylpiperidine (original) (raw)

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3,5-Dimethylpiperidines are chemical compounds with the formula C5H8(CH3)2NH. Two diastereomers exist: the achiral R,S isomer and the chiral R,R/S,S enantiomeric pair. 3,5-Dimethylpiperidine is a precursor to tibric acid. The compound is typically prepared by hydrogenation of 3,5-dimethylpyridine. Both diastereomers also arise from the reduction of 3,5-dimethylpyridine with lithium triethylborohydride.

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dbo:abstract 3,5-Dimethylpiperidines are chemical compounds with the formula C5H8(CH3)2NH. Two diastereomers exist: the achiral R,S isomer and the chiral R,R/S,S enantiomeric pair. 3,5-Dimethylpiperidine is a precursor to tibric acid. The compound is typically prepared by hydrogenation of 3,5-dimethylpyridine. Both diastereomers also arise from the reduction of 3,5-dimethylpyridine with lithium triethylborohydride. (en)
dbo:alternativeName 3,5-Lupetidine (en)
dbo:iupacName 3,5-Dimethylpiperidine (en)
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dbo:wikiPageWikiLink dbr:Enantiomer dbr:Lithium_triethylborohydride dbc:Piperidines dbr:Chemical_compound dbr:Chirality_(chemistry) dbr:2,6-Dimethylpiperidine dbr:Tibric_acid dbr:Piperidine dbr:Diastereomers
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dbp:imagename Structure of 3,5-dimethylpiperidine (en)
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dct:subject dbc:Piperidines
gold:hypernym dbr:Compounds
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rdfs:comment 3,5-Dimethylpiperidines are chemical compounds with the formula C5H8(CH3)2NH. Two diastereomers exist: the achiral R,S isomer and the chiral R,R/S,S enantiomeric pair. 3,5-Dimethylpiperidine is a precursor to tibric acid. The compound is typically prepared by hydrogenation of 3,5-dimethylpyridine. Both diastereomers also arise from the reduction of 3,5-dimethylpyridine with lithium triethylborohydride. (en)
rdfs:label 3,5-Dimethylpiperidine (en)
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