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"Friendly" synthesis of Benzyl Dimethyl Carbinol
just do a grignard reaction between benzyl bromide and acetone
6-10-2018 at 07:43
by: CuReUS
molecule synth
[rquote=540994&tid=93842&author=Assured Fish]I also do not see five chiral centres, havent a ...
6-10-2018 at 07:23
by: CuReUS
molecule synth
[rquote=539730&tid=93842&author=Jackson]Just to clear things up im not working at a univeris ...
1-10-2018 at 22:07
by: CuReUS
molecule synth
[rquote=539575&tid=93842&author=Assured Fish]Ive been researching how one could go about pre ...
1-10-2018 at 05:04
by: CuReUS
molecule synth
While trying to come up with the route I suggested in the previous page,I faced a dilemma about whic ...
30-9-2018 at 10:51
by: CuReUS
molecule synth
[rquote=538560&tid=93842&author=Assured Fish]is it possible for an alcohol to react in an al ...
29-9-2018 at 08:46
by: CuReUS
molecule synth
I came up with a modified version of fish's route ,aka the fureus route :D
the starting compound is ...
28-9-2018 at 08:25
by: CuReUS
Tired of reporting spam
[rquote=538746&tid=16937&author=streety]
There is a lot of overlap so I doubt much could be ...
27-9-2018 at 06:26
by: CuReUS
molecule synth
[rquote=538223&tid=93842&author=Assured Fish][u]Step #2[/u]
Simply acid calatysed eliminati ...
25-9-2018 at 23:15
by: CuReUS
molecule synth
the easiest way would be to reduce 1,5-pyracenedione (CAS no - 155143-87-6).Sadly I don't know how , ...
24-9-2018 at 22:07
by: CuReUS
Tired of reporting spam
anti spam measures - [url]https://web.archive.org/web/20151125135503/http://www.ninjapost.com/blog/9 ...
23-9-2018 at 02:19
by: CuReUS
Any ideas to passivate stainless steel against chlorine?
according to pg 60 this book - [url]https://library.sciencemadness.org/library/books/ignition.pdf[/u ...
17-9-2018 at 06:42
by: CuReUS
Eschweiler-Clarke reaction with protected amines
[rquote=533628&tid=90957&author=idk]Does the reaction proceeds with N-acyl protected amines[ ...
7-9-2018 at 08:58
by: CuReUS
Benzoic Acid Synthesis options
Go through the benzaldehyde thread.Most of the methods to make benzaldehyde give benzoic acid if ove ...
7-9-2018 at 04:44
by: CuReUS
Synthesis of longer chain tertiary alcohols
[rquote=532232&tid=15171&author=12thealchemist]Since this post, I gave the idea more thought ...
5-9-2018 at 04:48
by: CuReUS
Diphenylamine via Friedels-Craft-Alkylation?
[rquote=533095&tid=90510&author=wildfyr]You could try to deprotonate aniline with BuLi[/rquo ...
5-9-2018 at 04:39
by: CuReUS
Benzene synthesis
[rquote=532560&tid=325&author=digga]Once I have the product gin clear and dry, I will procee ...
1-9-2018 at 06:40
by: CuReUS
Synthesis of longer chain tertiary alcohols
[rquote=518169&tid=15171&author=12thealchemist]What if one used a bridgehead alcohol, for ex ...
20-8-2018 at 04:08
by: CuReUS
Preparing Grignard Reagents from 3-Bromopropylamine hydrobromide and other Compounds
[rquote=528864&tid=87735&author=VSEPR_VOID]Do you have any publications or articles relating ...
13-8-2018 at 03:47
by: CuReUS
anyone have experience forming grignards from chlorobenzene
[rquote=528899&tid=87827&author=draculic acid69]...if there are any tips or tricks to formin ...
13-8-2018 at 03:27
by: CuReUS
Acetic anhydride preparation
[rquote=528799&tid=9&author=clearly_not_atara]It appears that in the BV oxidation of diacety ...
13-8-2018 at 03:05
by: CuReUS
Preparing Grignard Reagents from 3-Bromopropylamine hydrobromide and other Compounds
[rquote=528751&tid=87735&author=VSEPR_VOID]What about :
Reaction of CH2=CHCH2MgCl with C60 ...
12-8-2018 at 03:13
by: CuReUS
Acetic anhydride preparation
[rquote=528655&tid=9&author=Waffles SS]5,4 g Diacetyl (63 Millimole) wurden in 500 cm3 Ather ...
12-8-2018 at 01:20
by: CuReUS
List some BAD chemistry YouTube videos
hilarious video,almost replicated the hindenburg :D [url]https://youtu.be/2-eMOCMDQj8?t=248[/url]
11-8-2018 at 02:00
by: CuReUS
Acetic anhydride preparation
why not do a baeyer-villiger on diacetyl to get AA ? -[url]https://books.google.co.in/books?id=AcpPy ...
11-8-2018 at 01:48
by: CuReUS
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