Synthesis and enantiomeric excess determination of (6S)-1-(trimethylsilyloxy)-6-(N-methyl-N-benzyloxycarbonylamino)-cyclohexene
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Add time:07/14/2019 Source:sciencedirect.com
The title compound was obtained with high regioisomeric and enantiomeric purity starting from the tartrate salt of (1S,2S)-1-hydroxy-2-methylaminocyclohexane. The determination of the enantiomeric excess both of the title compound and of its precursor (2S)-2-(N-methyl-N-benzyloxycarbonylamino)cyclohexanone was determined by NMR experiments with chiral shift reagents.
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Next:Efficient synthesis of (R)-6-benzyloxycarbonylamino-1-methyl-4-(3-methyl-benzyl)hexahydro-1,4-diazepine. 2. Novel formation of hexahydro-1,4-diazepine ring using 1,2,3-trisubstituted aminopropane derivative and glyoxal) - 【Back】【Close 】【Print】【Add to favorite 】
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