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)
Synthesis of the semi-rigid analogues of prothiadene and dithiadene as potential antidepressant and antihistamine agents: 11-[2-(dimethylaminomethyl)cyclohexylidene]-6,11-dihydro- dibenzo[b,e]thiepins and 4-[2-(dimethylaminomethyl)-cyclohexylidene]-4,9-di
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Polivka,Holubek,Svatek,et al.
p. 1078 - 1088
(2007/10/02)
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