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Offlinepsilocybian
enthusiast
Registered: 10/19/00
Posts: 153
Last seen: 23 years, 1 month
Chemistry Question
    #488856 - 12/12/01 03:35 PM (23 years, 6 months ago)

Ok, I dabble in a little organic chemistry, and I am aware of several synthetic routes to shrooms akaloids, but my main question is, how the hell does a shroom do it?

How the hell does it even form even an indole ring with nutrients water and air?

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OfflineHumidity
Mad Scientist
Registered: 04/01/00
Posts: 358
Loc: Somewhere in Northeast OH
Last seen: 21 years, 4 months
Re: Chemistry Question [Re: psilocybian]
    #488970 - 12/12/01 05:19 PM (23 years, 6 months ago)

Check out this link. From there it is futher processed into the good stuff.


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_____________________________________________________________________________________
"The greatest enemy of knowledge is not ignorance, it is the illusion of knowledge." -Stephen Hawking

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Offlinepsilocybian
enthusiast
Registered: 10/19/00
Posts: 153
Last seen: 23 years, 1 month
Re: Chemistry Question [Re: Humidity]
    #489795 - 12/13/01 12:12 PM (23 years, 6 months ago)

WOOF! The shrooms goes through a lot just to even make tryptophan.

I was thinking that since shrooms made these compounds from basic materials, someone might be able to replicate that in a laboratory. But forget it, I'd rather stick to starting with IAA or tryptophan any day.

I am still interested though. Even though your link gave the reaction mechanisms, it doesn't provide any details. Got any more links?

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OfflineHumidity
Mad Scientist
Registered: 04/01/00
Posts: 358
Loc: Somewhere in Northeast OH
Last seen: 21 years, 4 months
Re: Chemistry Question [Re: psilocybian]
    #489879 - 12/13/01 01:17 PM (23 years, 6 months ago)

There are synthetic ways to make psilocin, but you will need a laboratory to do it. And you will need to become a chemist because if you don't know what you are doing you are going to either blow yourself up or kill someone with a chemical that you make that is not psilocin. Leave to work up to the fungus they are the greatest chemists of them all.


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_____________________________________________________________________________________
"The greatest enemy of knowledge is not ignorance, it is the illusion of knowledge." -Stephen Hawking

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Offlineaka
newbie
Registered: 12/17/01
Posts: 38
Last seen: 23 years, 4 months
Re: Chemistry Question [Re: Humidity]
    #494921 - 12/18/01 02:29 PM (23 years, 5 months ago)

for sure, not only is nature a better chemist for somehting like that, but it's also a lot cheaper to let that nature take its course than to try to make l_tryptophan yourself

i've known of ppl who even with their own labs and lots of experience, have had to waste a lot of money (thousands) b4 the finished product was achieved.

think of it this way, gardenin is easier than chemistry, thus a large grow room is more feasable (and easier to conceal) than a small lab. not to mention the equipment required is 100x cheaper and easier to obtain and no funny questions

let us focus on the casings :)

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Offlinebiggwigg
member
Registered: 10/24/01
Posts: 112
Loc: PA
Last seen: 5 years, 10 days
Re: Chemistry Question [Re: aka]
    #495042 - 12/18/01 04:23 PM (23 years, 5 months ago)

you might as well make lsd or pcp hell of a lot cheaper not to mention easier


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I have only been wrong one time in my life.
thats when i thought i was wrong.
If its not a rave its not a party

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Invisiblealtarego
member
Registered: 10/25/01
Posts: 130
Re: Chemistry Question [Re: biggwigg]
    #495132 - 12/18/01 06:13 PM (23 years, 5 months ago)

Much organic chemistry is complicated and dangerous. The synthesis of psilocybin is especially hard, since it is 4-substituted and has that free hydroxyl group there.

It is basically DMT with the 4-OH, but DMT is two steps from a common precursor, psilocybin is at least six, and the precursor ain't that common. Better to let the mushroom do the work for you.

But if you are still interested in the theory, try "Improvements to the Synthesis of Psilocybin
and a Facile Method for Preparing the O-Acetyl Prodrug of Psilocin" by David E. Nichols and Stewart Frescas; Synthesis No. 6, 935-938 (1999)

- AE

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