Piperidine Derivatives. IV. 1,3-Disubstituted-4-aryl-4-acyloxy Piperidines
A. ZIERING, ALEX MOTCHANE, JOHN LEE;
J. Org. Chem.; 1957; 22(11); 1521-1528.
Abstract: On the basis of the infrared spectra of a-1,3-dimethyl-4-phenyl-4hydroxypiperidine and beta-1,3-dimethyl-4-phenyl-4-hydroxypiperidine, the a-form was tentatively designated cis and the beta-form trans with respect to H and OH. It was also shown that the alpha and beta forms of 1-methyl-3-R-4-phenyI-4-propionoxypiperidine (R = ethyl, allyl, crotyl) can be distinguished by several bands in the infrared. Other esters have been prepared where R is butyl, propyl, hexyl, and benzyl. All of the esters have been examined for their analgesic activity.
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Full-text: http://pharmacist8.tripod.com/Piperidine_Derivatives.pdf (http://pharmacist8.tripod.com/Piperidine_Derivatives.pdf)
Post 438046 (https://www.thevespiary.org/talk/index.php?topic=9742.msg43804600#msg43804600)
(Megatherium: "Hey ASSHOLE, yeah you pharmacist", Methods Discourse)
I'm pretty certain that I've prepared more psychoactive materials than you. Maybee you could show me your own research, please do Mr. Nichols.
If bringing the interesting articles to the hive is parasiting then this place is full of parasites...
You seem to have schizophrenic tendencies: Post 436990 (https://www.thevespiary.org/talk/index.php?topic=12205.msg43699000#msg43699000)
(Megatherium: "Indeed, this is VERY interesting.", Novel Discourse) If I wasn't parasiting you wouldn't have anything to bookmark you piece of shit...
Now I get it, he thought that I saw the ref he gave in Bwiti's thread and hurried to steal a karma point from him.. LOL, you are pathetic! I didn't even open that thread.
Check out the last reference listed in Future Synthetic Drugs of Abuse by Donald A. Cooper, you loser... Here: https://www.thevespiary.org/rhodium/Rhodium/chemistry/future_drugs.html (https://www.thevespiary.org/rhodium/Rhodium/chemistry/future_drugs.html)
Next time, don't post stoned and you might remember what journal you are refering to...