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Diamines alkylation
[rquote=451319&tid=66478&author=morsagh]I can´t find any reference to dialkylation of diami ... |
10-6-2016 at 01:30
by: CuReUS |
Diamines alkylation
zhiang is right,tertiary amine will be favoured.And bulky substituents favor secondary because they ... |
9-6-2016 at 07:55
by: CuReUS |
diiodomethane
[rquote=451224&tid=14235&author=Boffis]
The main issue I encountered seemed to be the prote ... |
9-6-2016 at 01:57
by: CuReUS |
4-Nitrochlorobenzene synhtesis
[rquote=450771&tid=66409&author=gboneu] i'm afraid that i'd tried the synthesis of aniline b ... |
9-6-2016 at 01:43
by: CuReUS |
4-Nitrochlorobenzene synhtesis
[rquote=451060&tid=66409&author=gboneu]I guess i will have to get aniline [/rquote]
If you ... |
8-6-2016 at 01:38
by: CuReUS |
Aniline
[rquote=450927&tid=65862&author=CRUSTY]
I recall reading somewhere that in Japan somewhere, ... |
6-6-2016 at 05:16
by: CuReUS |
Methyldichloramine
there are other ways to make the target compound
1. using TCCA - [url]http://www.sciencemadness.org ... |
5-6-2016 at 06:27
by: CuReUS |
Pyrrolidine/Putrescine?
according to this german paper,both pyrrolidine and putrescine will be formed when NH[sub]3[/sub] is ... |
5-6-2016 at 06:05
by: CuReUS |
4-Nitrochlorobenzene synhtesis
You could do this :
1.nitrobenzene to chlorobenzene - [url]http://pubs.acs.org/doi/abs/10.1021/jo00 ... |
4-6-2016 at 23:01
by: CuReUS |
Alkylation of terminal alkyne on alcohol
Please give more info about the compound you want to synthesis instead of giving references.Maybe yo ... |
4-6-2016 at 02:33
by: CuReUS |
Synthesis of propanamide
Another way to make it is via a willgerodt reaction on acetone
[url]http://pubs.acs.org/doi/abs/10 ... |
3-6-2016 at 04:51
by: CuReUS |
Disproportionation of phenylphosphinic acid: OTC triphenylphosphine?
I found two alternatives to TPP. One is the non-ingenious tributylphosphine but the other one is lit ... |
3-6-2016 at 04:43
by: CuReUS |
mystery stinking compound
[rquote=450522&tid=66390&author=zed]we might be looking at the Willgerodt Reaction[/rquote]
... |
3-6-2016 at 00:52
by: CuReUS |
mystery stinking compound
You have replicated in a scientific way,an age-old recipe to make stink bombs
the S reacted with ... |
1-6-2016 at 02:51
by: CuReUS |
Disproportionation of phenylphosphinic acid: OTC triphenylphosphine?
[rquote=450469&tid=65473&author=clearly_not_atara]
That leaves the question of how to get ... |
1-6-2016 at 02:20
by: CuReUS |
Disproportionation of phenylphosphinic acid: OTC triphenylphosphine?
found four high yielding procedures,but most likely not OTC
[url]http://pubs.acs.org/doi/abs/10.10 ... |
31-5-2016 at 01:04
by: CuReUS |
Styrene to Acetophenone
first of all,thanks for finding such a good paper,I don't understand the reason for this hate debat ... |
29-5-2016 at 03:06
by: CuReUS |
diiodomethane
I have had this question for a long time. Could you reduce iodoform to DIM using an alkaline glucose ... |
29-5-2016 at 02:54
by: CuReUS |
Pyrimethamine Synthesis?
first of all,thank you so much for reviving the thread,I thought it died
[rquote=450252&tid=6 ... |
29-5-2016 at 01:37
by: CuReUS |
Pyrimethamine Synthesis?
I was thinking about this synthesis and it dawned upon me that the reason we got stuck was because a ... |
23-5-2016 at 23:01
by: CuReUS |
andrafinil
[rquote=449660&tid=66274&author=CrossxD]but can I moke thioglycolic acid from chlor acetec a ... |
22-5-2016 at 08:31
by: CuReUS |
List some BAD chemistry YouTube videos
[rquote=449436&tid=48892&author=j_sum1]
The problem is that it appears reasonable and looks ... |
19-5-2016 at 05:55
by: CuReUS |
andrafinil
there is another route you could try
1.synthesis of 2-benzhydrylsulfanylacetic acid from benzhydrol ... |
18-5-2016 at 04:46
by: CuReUS |
Aquarium Tank uses - ideas?
[rquote=448949&tid=66246&author=RogueRose][color=Red]glass[/color] aquarium...Chlor-[color=R ... |
15-5-2016 at 03:09
by: CuReUS |
Oxidation of styrene to phenylacetaldehyde
[rquote=448756&tid=22421&author=clearly_not_atara]
Big problem with DMSO oxidations is the ... |
13-5-2016 at 09:48
by: CuReUS |
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