Talk:Nortilidine

Optical purity
Optical Activity of nortilidine is specified in the image. I haven't seen any evidence that the body only metabolizes one of the two (trans) isomers used medically. The patent route does first isolate the D(trans)isomer, but this isn't the only process for the manufacture of nortilidine. When sold as a research material, nortilidine is not optically pure. — Preceding unsigned comment added by 86.30.243.179 (talk) 11:56, 21 July 2011 (UTC)

Image
The image is of the INACTIVE isomer - can some one PLEASE FIX THIS MAJOR ERROR!!!!!!! — Preceding unsigned comment added by 86.30.243.179 (talk) 15:29, 22 March 2012 (UTC)


 * Maybe both isomers of tilidine are metabolized but maybe not - this image could be worse than useledd - it doesn't even match the IUPAC name!!! — Preceding unsigned comment added by 86.30.243.179 (talk) 10:00, 5 April 2012 (UTC)


 * I have replaced the image with one that matches the isomer shown on PubChem for nortilidine, I'm hoping this is the correct one :-)  Meodipt (talk) 23:17, 5 May 2012 (UTC)

Derivatives
Some interesting discussion on nortilidine derivatives and nortilidine synthesis offsite here. Nagelfar (talk) 17:00, 11 September 2012 (UTC)

Personal Communication with Derek P. Reynolds
Could i get some more information on this? Anyways how does "personal communication" suffice as a reference? Etr83441 (talk) 19:59, 8 December 2023 (UTC)