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Originally posted by gwh200 View PostHe's not that sort of lawyer...some geek vs some geek.
but anyways, welcome back Henry...it's been dull.
This month I shall mostly be showing that, given the anticholinesterase racemic mixture (+/-)-N-ethyl-3-[(1-dimethylamino)ethyl]-N-methyl-phenyl-carbamate in its hydrochloride form, it would have been obvious for the skilled man as at 1987 to resolve the racemate into its enantiomers in free base or acid addition salt form, whether or not the increased activity of the isomeric form would have been unexpected given that the dialylaminoalkyl side chain which contains the optically active centre would have been understood to have been mainly responsible for the acetylcholinesterase inhibiting activity of the phenyl carbamate.
What's geeky about that?
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Nothing.
I meant geeky, in an open toe sandal, bought all your clothes from C&A type of way.
That all does sound remarkably, like a chlorine salt thing...which we use tons of...but I wouldn't know, not being a nerdy geek!Non intercooled nothing.
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Originally posted by gwh200 View PostNothing.
I meant geeky, in an open toe sandal, bought all your clothes from C&A type of way.
That all does sound remarkably, like a chlorine salt thing...which we use tons of...but I wouldn't know, not being a nerdy geek!
brogues possibly
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Originally posted by gwh200 View PostNothing.
I meant geeky, in an open toe sandal, bought all your clothes from C&A type of way.
That all does sound remarkably, like a chlorine salt thing...which we use tons of...but I wouldn't know, not being a nerdy geek!
I have never, ever, bought anything from C&A. Though I have on occasion been called both...
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Originally posted by flounderbout View PostGeeky?
This month I shall mostly be showing that, given the anticholinesterase racemic mixture (+/-)-N-ethyl-3-[(1-dimethylamino)ethyl]-N-methyl-phenyl-carbamate in its hydrochloride form, it would have been obvious for the skilled man as at 1987 to resolve the racemate into its enantiomers in free base or acid addition salt form, whether or not the increased activity of the isomeric form would have been unexpected given that the dialylaminoalkyl side chain which contains the optically active centre would have been understood to have been mainly responsible for the acetylcholinesterase inhibiting activity of the phenyl carbamate.
What's geeky about that?
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