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Products of reaction
[rquote=466890&tid=70876&author=Neme]
It is a two step synthesis which first step is heatin ... |
17-11-2016 at 09:18
by: CuReUS |
Products of reaction
[url]https://en.wikipedia.org/wiki/Adams%27s_catalyst#Preparation[/url]
PtO[sub]2[/sub] is platinum ... |
17-11-2016 at 06:43
by: CuReUS |
MITSUNOBU REACTION WITH PRIMARY AMIDES
according to wiki,for the mitsunobu reaction to work,the nucleophile must have a pKa less than 15.Fo ... |
17-11-2016 at 02:45
by: CuReUS |
List some BAD chemistry YouTube videos
another crazy video.His hand got "reduced" to nothing - [url]https://www.youtube.com/watch?v=ESqE1gT ... |
17-11-2016 at 01:04
by: CuReUS |
Trying to synthesize 1-iodobutane
[rquote=465993&tid=70660&author=siam65]Actually i cannot use elemental iodine in my reaction ... |
5-11-2016 at 00:31
by: CuReUS |
Trying to synthesize 1-iodobutane
how about using Al foil,I[sub]2[/sub] and n-butanol ? |
4-11-2016 at 01:14
by: CuReUS |
List some BAD chemistry YouTube videos
[rquote=465843&tid=48892&author=ficolas][rquote=465748&tid=48892&author=j_sum1](Prob ... |
3-11-2016 at 04:11
by: CuReUS |
M-toluic Acid Chlorination
you can do a one pot conversion of carboxylic acid to amide using TCT.
[quote]Sodium hydroxide (9.7 ... |
3-11-2016 at 03:45
by: CuReUS |
2,4-DNPH in schools - overreaction
But why did the castlemaine guy have anti-personnel mines if he was just making firecrackers ? |
2-11-2016 at 03:58
by: CuReUS |
1,2-benzoquinone
[rquote=465666&tid=70607&author=morsagh]I want to do some hetero diels-alder reaction with 1 ... |
2-11-2016 at 02:54
by: CuReUS |
Secondary amine mannich condensation + ring formation.
[rquote=465514&tid=70391&author=bmays] The methyl won't be a problem,i have some boron tribr ... |
31-10-2016 at 04:44
by: CuReUS |
Secondary amine mannich condensation + ring formation.
[rquote=465447&tid=70391&author=bmays]So you're saying with MVK, one mole of formaldehyde, a ... |
29-10-2016 at 22:34
by: CuReUS |
Secondary amine mannich condensation + ring formation.
[rquote=465429&tid=70391&author=bmays]I'm interested in an unsubstituted ring though[/rquote ... |
29-10-2016 at 20:17
by: CuReUS |
Some gross stuff!
sorry I made a mistake.Dibromo acetylene gives you a headache,not diidoacetylene.But according to th ... |
28-10-2016 at 07:17
by: CuReUS |
Secondary amine mannich condensation + ring formation.
[rquote=465144&tid=70391&author=bmays]products derived from [color=Red]two[/color] molecules ... |
26-10-2016 at 20:26
by: CuReUS |
Synthesis of Allylbenzene
[rquote=465059&tid=9310&author=clearly_not_atara]I'm not sure that you can make p-toluenesul ... |
25-10-2016 at 22:47
by: CuReUS |
naphthoyl indole grignard question.
[rquote=464996&tid=70405&author=kineticz]My Problem: I do not have access to anhy Ethanol[/ ... |
25-10-2016 at 07:41
by: CuReUS |
Secondary amine mannich condensation + ring formation.
[rquote=464968&tid=70391&author=bmays]If a mannich condensation was carried out between dime ... |
25-10-2016 at 06:52
by: CuReUS |
Synthesis of Allylbenzene
[rquote=464940&tid=9310&author=Cryolite.]If cinnamaldehyde can be reduced to 3-phenylpropano ... |
25-10-2016 at 06:08
by: CuReUS |
Most practical way to oxidize a primary alcohol to an acid?
[rquote=464943&tid=70371&author=Melgar] Perhaps if done in an alkaline media, the acid will ... |
25-10-2016 at 05:16
by: CuReUS |
Most practical way to oxidize a primary alcohol to an acid?
see this thread -[url]http://www.sciencemadness.org/talk/viewthread.php?tid=29620[/url]
although th ... |
24-10-2016 at 09:20
by: CuReUS |
Synthesis of Allylbenzene
[rquote=464725&tid=9310&author=Maroboduus]Wouldn't using these various chloride Lewis acids ... |
22-10-2016 at 18:10
by: CuReUS |
microencapsulation of marquis reagent and others
[rquote=464730&tid=70248&author=j_sum1] I take issue with your philosophical stance[/rquote] ... |
22-10-2016 at 18:01
by: CuReUS |
Synthesis of Allylbenzene
[rquote=154375&tid=9310&author=Nicodem]alpha-resorcylic acid is commercially available and v ... |
22-10-2016 at 01:13
by: CuReUS |
Kaiser ninhydrin test: what's the point of the cyanide?
[quote]In the search for a more stable and soluble reducing agent we observed that potassium cyanide ... |
21-10-2016 at 19:50
by: CuReUS |
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