05-11-00 21:50
No 2949
I'm almost 100% sure that you can't but.. Is there any possibility of converting AMT(a-MethylTryptamine) to AET(a-EthylTryptamine?
(Stranger)
05-12-00 00:46
No 3017
Thought so :) Brain farts just happen ;) Do you know of any substitue for LAH?
It's fun programming your quantum computer!
(Hive Bee)
05-12-00 08:02
No 3145
I don't know of a direct substitute for LAH. But there is almost always an alternatice synthetic way. Think of the nitrostyrene reduction: Shulgin uses LAH all the time. but you can also do it with [NaBH4 + NiCl2] or electrolytically or first reduce the double bond with NaBH4, then the nitro group. Or you could go the phenylethanol --> phenylethyl-iodid --> PEA way... this is what I love about organic chemistry.
--psyloxy--
(Stranger)
05-12-00 21:04
No 3393
Yeh I just see DET. But it doesn't mean that it isn't illegal (I don't know Canadian laws that much).. They might have an analogue act?
http://canada.justice.gc.ca/FTP/EN/Laws/
"When I was young I played with legos. But now I am older and I play with atoms."