malvaxman
(Hive Bee) 05-22-02 01:47 No 312192 |
Is there any method... | Bookmark | ||||||
Is there any method to make pure enantiomeric d-meth which doesn´t involve natural products like l-ephedrine l-PAC? ....i guess the method which ofcours exists could be applicable in some research fascility but deffinitly not my kitchen or garage. /Thank you for your help |
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Rhodium (Chief Bee) 05-22-02 01:55 No 312199 |
Resolution instructions | Bookmark | ||||||
../rhodium /ampheta |
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PrimoPyro (Hive Prodigy) 05-22-02 02:06 No 312205 |
Just putting the word out | Bookmark | ||||||
There are also likely to be other possibilities involving organometallic syntheses. Many chiral agents have been developed for many syntheses involving these reactions. More information, I cannot produce, this is essentially all I know. My source (March's 5th) was very vague, and only consisting of about two sentences stating what I already stated. Many of these catalysts revolve around the syntheses of alcohols and amines, so it is likely that such methods exist and are applicable here. What they are, I do not know as of yet. PrimoPyro Vivent Longtemps La Ruche! How's my posting? Call 1-800-EAT-SHIT |
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lugh (Moderator) 05-22-02 02:16 No 312212 |
Methylbenzylamine | Bookmark | ||||||
You can also use reductive alkylation using methylbenzylamine as found in: ../rhodium /reducti Reductive Alkylation of alpha-Methylbenzylamine with 1-Phenyl-2-Propanone Followed by Hydrogenolysis: Nichols et al., Asymmetric Synthesis of Psychotomimetic Phenylisopropylamines, J. Med. Chem. 16(5) (1973) 480-3. This procedure offers a route to dextro-amphetamine from phenyl-2-propanone |
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Rhodium (Chief Bee) 05-22-02 02:19 No 312214 |
RMgX + CuI + Imine -> Amine 99% yield, 99% ee | Bookmark | ||||||
Synlett 651 (2002) has a large review article of stereospecific addition of organometallic reagents to imines to form optically pure amines. It even includes some 2,5-dimethoxyphenyl compounds. |
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PrimoPyro (Hive Prodigy) 05-22-02 02:34 No 312221 |
99% ee? | Bookmark | ||||||
99% ee? Does that mean 99% enantiomerically efficient by any chance? Just a wild guess. Vivent Longtemps La Ruche! How's my posting? Call 1-800-EAT-SHIT |
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Rhodium (Chief Bee) 05-22-02 03:01 No 312235 |
Enantiomeric excess (Rated as: Good Explanation) |
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Enantiomeric excess. A racemic mixture is 0% ee, and a pure optical isomer is 100% ee. A 99% ee mixture consists of 99.5% of one isomer and 0.5% of the other. Stupid unit, I know. |
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PrimoPyro (Hive Prodigy) 05-22-02 03:09 No 312240 |
Thank You | Bookmark | ||||||
I will remember this. The unit is ok, its value reminds me of the Proof system for alcohols, also redundant. PrimoPyro Vivent Longtemps La Ruche! How's my posting? Call 1-800-EAT-SHIT |
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