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• W2023779054 abstract "The acetylcholinesterase inhibition by enantiomers of exo- and endo-2-norbornyl-N-n-butylcarbamates shows high stereoselelectivity. For the acetylcholinesterase inhibitions by (R)-(+)- and (S)-(-)-exo-2-norbornyl-N-n-butylcarbamates, the R-enantiomer is more potent than the S-enantiomer. But, for the acetylcholinesterase inhibitions by (R)-(+)- and (S)-(-)-endo-2-norbornyl-N-n-butylcarbamates, the S-enantiomer is more potent than the R-enantiomer. Optically pure (R)-(+)-exo-, (S)-(-)-exo-, (R)-(+)-endo-, and (S)-(-)-endo-2-norbornyl-N-n-butylcarbamates are synthesized from condensations of optically pure (R)-(+)-exo-, (S)-(-)-exo-, (R)-(+)-endo-, and (S)-(-)-endo-2-norborneols with n-butyl isocyanate, respectively. Optically pure norborneols are obtained from kinetic resolutions of their racemic esters by lipase catalysis in organic solvent." @default.
• W2023779054 created "2016-06-24" @default.
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• W2023779054 date "2009-01-01" @default.
• W2023779054 modified "2023-10-17" @default.
• W2023779054 title "Synthesis of enantiomers ofexo-2-norbornyl-N-n-butylcarbamate andendo-2-norbornyl-N-n-butylcarbamate for stereoselective inhibition of acetylcholinesterase" @default.
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• W2023779054 doi "https://doi.org/10.1002/chir.20739" @default.
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