| Search |
| [Next Page] |
Selective Amination of Benzoic Acid
A general method for addition of an amino group to an aromatic compound would be to nitrate and then ... |
25-6-2012 at 15:24
by: UKnowNotWatUDo |
Copper acetate making iodine
First I believe you are confusing oxidation and reduction. Reduction of iodine would be changing ele ... |
11-6-2012 at 16:34
by: UKnowNotWatUDo |
Metal/acid reduction of benzoin
If you intend to try using zinc dust and hydrochloric acid for the reduction I wonder if the fine zi ... |
9-6-2012 at 07:03
by: UKnowNotWatUDo |
tryptophan to alpha methyl tryptamine
Yes the MeMgI route would certainly be simpler for most, but as the original poster seems to have a ... |
29-5-2012 at 10:49
by: UKnowNotWatUDo |
tryptophan to alpha methyl tryptamine
To prevent decomposition TO the imine (elimination)? Or to prevent decomposition OF the imine (hydro ... |
28-5-2012 at 09:32
by: UKnowNotWatUDo |
tryptophan to alpha methyl tryptamine
I'm not sure the Kochi reaction would work on tryptophan in the first place, but even if it did the ... |
26-5-2012 at 19:33
by: UKnowNotWatUDo |
Stannous Halides - Are they all reducing agents?
Speaking of stannous chloride, does anyone have any detailed reaction mechanisms for the reductions? |
23-5-2012 at 19:33
by: UKnowNotWatUDo |
Stannous Halides - Are they all reducing agents?
I know tin(II) bromide is indeed a reducing agent as well. I assume it will also reduce nitro compou ... |
22-5-2012 at 05:57
by: UKnowNotWatUDo |
Making hydrochloric acid
There are many different brands and each has a different concentration of HCl and different additive ... |
21-5-2012 at 02:40
by: UKnowNotWatUDo |
Making hydrochloric acid
What about just buying hardware store muriatic acid? |
21-5-2012 at 01:09
by: UKnowNotWatUDo |
Are amino groups oxidised in the same way hydroxy groups are?
He's saying that he has 4-aminophenol, which is the product you get when acetaminophen is hydrolyzed ... |
18-5-2012 at 14:53
by: UKnowNotWatUDo |
Boric Acid Catalyzed Amidation of Carboxylic Acids
In the reference you posted they state that 5 mol% boric acid catalyst was generally fine for most r ... |
11-3-2012 at 21:39
by: UKnowNotWatUDo |
It is possible to have H2SO4 this cold?
In the spirit of answering the original question, here is a link to graphs and tables of various pro ... |
5-3-2012 at 03:15
by: UKnowNotWatUDo |
It is possible to have H2SO4 this cold?
This reaction appears to me to be a rearrangement, or actually a series of rearrangements. Here's my ... |
4-3-2012 at 23:15
by: UKnowNotWatUDo |
NH3 (aq) or NH4OH
Entropy51, so many of your posts lately have been made up of snide, rude, and insulting remarks towa ... |
7-2-2012 at 02:02
by: UKnowNotWatUDo |
3,4-MD-Phenmetrazine
I hate to be the bearer of bad news, but your new reaction schemes have a few problems still. Take a ... |
30-12-2011 at 10:13
by: UKnowNotWatUDo |
Only L-ala and L-ser tripeptides?
Remember also that peptides have a "front" and a "back", so A-A-S is not the same peptide as S-A-A. |
9-12-2011 at 18:11
by: UKnowNotWatUDo |
Journal of amateur science
Nicodem, I didn't mean regulation was necessary because syntheses of illegal (in the US) compounds l ... |
29-11-2011 at 12:49
by: UKnowNotWatUDo |
Journal of amateur science
Your questions are all valid ones. And different people would have different answers for you. This i ... |
29-11-2011 at 05:32
by: UKnowNotWatUDo |
Journal of amateur science
I think this idea could be a really interesting and possibly long running project. The problem would ... |
29-11-2011 at 03:12
by: UKnowNotWatUDo |
reduction of MDP2NP
I wouldn't think so, but again I've never worked first hand with this compound or any of it's deriva ... |
14-11-2011 at 03:40
by: UKnowNotWatUDo |
reduction of MDP2NP
No worries, we all make typos. I have never run this particular reaction but from what I've read and ... |
14-11-2011 at 03:25
by: UKnowNotWatUDo |
reduction of MDP2NP
Do you mean the aminoalkane? |
14-11-2011 at 03:15
by: UKnowNotWatUDo |
S...O...S Help, can anybody tell me the CAS Number for this molecule??
Well then, that's the problem with not using IUPAC naming. People have to guess at what you are talk ... |
13-11-2011 at 22:15
by: UKnowNotWatUDo |
S...O...S Help, can anybody tell me the CAS Number for this molecule??
Around here pretty much every post that doesn't come with some kind of literature reference is put t ... |
13-11-2011 at 21:17
by: UKnowNotWatUDo |
| [Next Page] |
