motek: I would never give you a free guide, I was being sarcastic. You are totally delusional, what makes you think I would ever give a free guide to someone whos stated that A) they would never accept one B) has made outright lies in an attempt to lower my credibility and C) someone who would abandon logic and make himself look like an autistic 12 year old with an internet connection just to attempt to discredit me.
You are accusing me of deleting negative commends? You LITERALLY think that there is a huge conspiracy to hide negative reviews of me? How about the more simple alternative, there are very few people who purchased that have negative things to say. You act like dissonance has your back against me, he apologized and changed his stance after talking with me on this thread!
Looks like you did some googling and made a list of ergoloids, what exactly are you trying to prove?
Yes, some of those compounds can be broken down to lysergic acid used for LSD synthesis but almost none of them are available commercially and many of them are 100% unrealistic to use.
Most of those compounds are very very expensive and the ones available commercially in pill form contain doses around 1mg per pill, AKA 1000 pills per gram, before the weight loss of hydrolysis!
You are much better off using my method and producing 1 gram for every liter of fermentation broth.
your list of ergoloids means nothing! a few of them are even totally useless!
So your favorite ergoloid for LSD production is LYSERGOL?
You really don't know anything about organic chemisty except for how to copy and paste fancy looking names from the internet.
LYSERGOL is next to impossible to utilize! Lysergol requires a selective oxidation to convert the alcohol into a carboxylic acid. Do you know how hard it is to find an oxidation agent that will leave the rest of that fragile molecule alone and only oxidize the alcohol group? You realize that this was only recently accomplished in very low yields in a professional lab right? It was done as a proof of concept and would never be practical in any other way. TOTAL GARBAGE. Only looks good to someone that has never done any synthesis before in their life.
" **AND I 'forgot' to ask you how you about " amine protection"
becoz you will have to protect your amine first and then deprotect it. "
Oh really? thats funny because Im pretty sure that lysergic acid does not have any reactive amines in this sense, just a tertiary and secondary amine in a ring. They don't need protection at all using peptide coupling. This is basic stuff motek, you are really showing your ignorance off here.
You are failing at even copying and pasting information! We should talk chemistry more often!
idiot.
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