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What can N2O (nitrous oxide, dinitrogen monoxide) be used for?
I recently read a russian article in another thread in which they used N[sub]2[/sub]O for oxidising ... |
6-4-2016 at 04:37
by: CuReUS |
Simple(er)Aluminum Isopropoxide prep experiment for later this week.
not related to this thread but IMHO,there are many other OTC reducing and oxidising agents that are ... |
1-4-2016 at 05:07
by: CuReUS |
Green Synthesis of 3-methyl-heptan-3-ol from common materials
Instead of using BuBr,why don't you try making BuCl, it can be easily made by the TCT/DMF method,and ... |
31-3-2016 at 03:59
by: CuReUS |
Green Synthesis of 3-methyl-heptan-3-ol from common materials
you might be able to increase the yield if you used 2-methyl THF instead of THF
[url]http://pubs.ac ... |
29-3-2016 at 05:29
by: CuReUS |
Boxwood odor
the book which talks about the addition of acetic acid to alkene is - de klein,W.J in "organic synt ... |
26-3-2016 at 01:10
by: CuReUS |
Boxwood odor
I was thinking about removing a few more steps and one of the ways that can be done is doing a one p ... |
25-3-2016 at 02:38
by: CuReUS |
Preparation of STABLE colloidal gold
this might be useful
[url]https://en.wikipedia.org/wiki/Gold_number[/url] |
24-3-2016 at 04:16
by: CuReUS |
Boxwood odor
[quote] One step from acetone to make which intermediate? thioacetone?[/quote]
very clever reaction ... |
23-3-2016 at 05:14
by: CuReUS |
Pimelic Acid Synthesis?
[rquote=442735&tid=65674&author=SmellNoEvil]
I have looked through the patents cited on the ... |
22-3-2016 at 01:19
by: CuReUS |
Boxwood odor
after a lot of searching,I have finally found a method to convert the ketone to thiol via reduction ... |
19-3-2016 at 03:21
by: CuReUS |
Boxwood odor
[rquote=442267&tid=65586&author=moonfisher]
I won't be working with organolithium just yet. ... |
18-3-2016 at 02:50
by: CuReUS |
4-Amino-1-phenethylpiperidine | CAS: 51448-56-7
[rquote=442060&tid=65615&author=solo]......a very nice approach Atara[/rquote]
but isn't it ... |
17-3-2016 at 06:00
by: CuReUS |
Boxwood odor
[rquote=441976&tid=65586&author=moonfisher]
Im planning to make the hydroxybutanone this we ... |
16-3-2016 at 05:56
by: CuReUS |
ethyl acetoacetate synthesis
[rquote=441989&tid=65602&author=clearly_not_atara]
It can actually take more than a week fo ... |
16-3-2016 at 05:22
by: CuReUS |
Boxwood odor
I have come up with some routes to make 4-hydroxybutan-2-one
1. from 2-methyloxetane: reaction o ... |
15-3-2016 at 05:58
by: CuReUS |
ethyl acetoacetate synthesis
NaNH[sub]2[/sub] on ethylacetate gives ethylacetoacetate. Maybe the same reaction could be done usin ... |
14-3-2016 at 06:29
by: CuReUS |
Boxwood odor
[rquote=441667&tid=65586&author=CuReUS]
4.conversion of ketone to thiol via the thioketal t ... |
14-3-2016 at 05:33
by: CuReUS |
Boxwood odor
[rquote=441623&tid=65586&author=moonfisher]
3-mercaptohexyl acetate- seems easy enough: 3- ... |
13-3-2016 at 06:09
by: CuReUS |
lithium phenylacetylide
[rquote=441441&tid=65213&author=clearly_not_atara] Be aware that phenylacetylene is not a pr ... |
12-3-2016 at 05:10
by: CuReUS |
Fétizon Reagent regeneration ?
[rquote=441100&tid=65529&author=clearly_not_atara]Silver carbonate on celite (silica) probab ... |
8-3-2016 at 04:57
by: CuReUS |
Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation
the formic acid method is amazing.I wonder why no one mentioned it before
I was thinking about it a ... |
1-3-2016 at 06:23
by: CuReUS |
Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation
[rquote=440356&tid=65213&author=Dope Amine]
Alpha-ketol rearrangements: According to the " ... |
29-2-2016 at 06:01
by: CuReUS |
Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation
[rquote=440129&tid=65213&author=Dope Amine] all of my subsequent reading has indicated that ... |
28-2-2016 at 03:29
by: CuReUS |
Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation
sorry to rain on your parade atara,but I don't think you read my post carefully, alpha ketol rearran ... |
26-2-2016 at 05:52
by: CuReUS |
Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation
[rquote=437466&tid=65213&author=Dope Amine]
BUT, the concern is that given this product i ... |
26-2-2016 at 03:45
by: CuReUS |
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