Talk:Geosmin

Latest comment: 5 years ago by Mykhal in topic Octahydronapthalene?

Needs stereochemistry edit

Structural formula does not show stereochemistry, which is critical to correctly describe natural products. AcidFlask 21:01, 30 September 2007 (UTC)Reply

I found a better image on Commons and replaced the current one with it. --Ed (Edgar181) 21:15, 30 September 2007 (UTC)Reply


Geosmin (geo·​smin | \ jē-ˈō-smən) was first described by Gerber,N. N. and Lechevalier, H. A. 1965.Geosmin, an earthy-smelling substance isolated from actinomycetes. Appl. Microbiol. 13: 935 - 938. —Preceding unsigned comment added by Elicsiegel (talkcontribs) 23:53, 5 June 2008 (UTC)Reply

sorry guys I know I should have started another subsection on the discussion but I have no idea how.. and I would put one of those [citation needed] things in the article but again.. not the most computer savvy here.. anyway is there a citation for this?

'The human nose is extremely sensitive to geosmin and is able to detect it at concentrations as low as 5 parts per trillion.'

thanks —Preceding unsigned comment added by 58.111.67.243 (talk) 04:28, 16 June 2009 (UTC)Reply

Argosmin edit

... a.k.a. geosmin's odourless breakdown product. Structure is here if anyone wants to have a shufti. I'll draw it and add it to the article over the next few weeks since I have exams next week. Brammers (talk/c) 08:20, 13 June 2010 (UTC)Reply

Octahydronapthalene? edit

Surely it is heptahydronapthalene? I have emailed various institutions, I'll wait until I hear back to edit it. — Preceding unsigned comment added by Brocerius (talkcontribs) 11:37, 16 May 2012 (UTC)Reply

Oop! Finally managed to find an organic chemist, sorry. Ignore this Brocerius (talk) 12:04, 16 May 2012 (UTC)Reply

@Brocerius: It was very relevant question, yet more if you meant decahydronaphthalene instead. I wonder what arguments did you get, except that name is from chemical databases and/or software generated. I bet I can then get you an counterargument. The organic nomenclature became self-inconsistent. Many trivial names were adopted, I wonder why decalin not. —Mykhal (talk) 09:40, 16 June 2018 (UTC)Reply
.. well, OK, in this case there was oviously one "implicit (di)hydrogenation" because of the substitution at the naphthalene "condensation joint" carbons with no hydrogens. —Mykhal (talk) 09:58, 16 June 2018 (UTC)Reply