Absolute configuration and local anaesthetic activity of cis and trans 2-dimethylaminomethyl-cyclohexyl benzoates
All the four stereoisomers of 2-dimethylaminomethyl-cyclohexyl benzoate (enantiomers of 4 and 5) were prepared in optically pure state and their absolute configurations determined by chiroptical methods and genetic correlations. The configurational assign
Nemes,Kajtar,Kajtar,Karpati,Nador
p. 1081 - 1084
(2007/10/02)
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