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Amination of tertiary alkyl halide
Finally tracked down some old Ritter references.
Here is an example from one of the papers:
N- ... |
27-3-2013 at 11:13
by: ctrade |
Amination of tertiary alkyl halide
[rquote=279010&tid=23757&author=Nicodem][rquote=279008&tid=23757&author=ctrade]Id li ... |
25-3-2013 at 22:01
by: ctrade |
Amination of tertiary alkyl halide
I will do as advised and use either HCN generated in situ or acetonitrile with my alcohol. Ill post ... |
25-3-2013 at 11:54
by: ctrade |
Aromatic bromination with NBS
I guess I will answer myself. N-iodosuccinimide will not work as stated in my previous post. In orde ... |
24-3-2013 at 13:03
by: ctrade |
Aromatic bromination with NBS
5 grams (23mmol) of 2,4-dimethoxyphenylethylamine HCL was dissolved in 35ml GAA and 6.3g (28mmol) N- ... |
24-3-2013 at 11:13
by: ctrade |
Amination of tertiary alkyl halide
Thank you very much Nicodem. I have changed my original plan and will post it later. It will give me ... |
22-3-2013 at 12:00
by: ctrade |
Aromatic bromination with NBS
The original procedure has always worked fine for me with the hydrochloride salt of the amine. Almos ... |
22-3-2013 at 11:58
by: ctrade |
Amination of tertiary alkyl halide
[rquote=278485&tid=23757&author=Nicodem][rquote=278405&tid=23757&author=ctrade]I am ... |
20-3-2013 at 15:52
by: ctrade |
Amination of tertiary alkyl halide
[rquote=278408&tid=23757&author=Prometheus23]Why do you keep saying tertiary alkyl halide? I ... |
19-3-2013 at 13:54
by: ctrade |
Amination of tertiary alkyl halide
I am trying to synthesize napthyl isopropylamine from napthyl isopropyl chloride but keep hitting wa ... |
19-3-2013 at 13:19
by: ctrade |
