| Search |
| [Next Page] |
help... Endnote forces me to do the dirty work myself
you're right.
I needed to search again and export the results as a "tagged .txt file" |
18-6-2007 at 11:42
by: Dr. Beaker |
help... Endnote forces me to do the dirty work myself
Hi all,
I have many articles as pdf files sorted in folders.
Is there a way endnote can read tho ... |
16-6-2007 at 12:14
by: Dr. Beaker |
Complexing of Group 4 and Group 5 Elements
This is such a wide subject...
Ti (IV) for example can be tetra coordinative (TiCl4, TiOMe4, TiCPCl ... |
4-6-2007 at 13:17
by: Dr. Beaker |
Aldehyde to nitrile
I have'nt tried but as stated in the J. Org. Chem. 2003 article the intermediate is an N iodo imine ... |
4-6-2007 at 05:23
by: Dr. Beaker |
Aldehyde to nitrile
Glad Ziqquratu was able to give you the pdf's. I just didn't had the time, sorry.
Anyway, if you wa ... |
2-6-2007 at 12:29
by: Dr. Beaker |
Aldehyde to nitrile
[quote][i]Originally posted by Sauron[/i]
I'm highly skeptical of the transformation of aldehyde to ... |
1-6-2007 at 06:51
by: Dr. Beaker |
synthetic chalange regarding oligo-ethylene glycol
Thank you for the very helpfull info.
"The advantage of working with the tetraglycol ditosylate and ... |
29-5-2007 at 08:12
by: Dr. Beaker |
Dangers of sodium, unexpected result
great movie  . very counter safty...
if you look very cearfully you see that the explossion is ind ... |
28-5-2007 at 15:44
by: Dr. Beaker |
synthetic chalange regarding oligo-ethylene glycol
I agree with you in regard to the last comment.
But about the first - what side products do you mea ... |
24-5-2007 at 12:37
by: Dr. Beaker |
synthetic chalange regarding oligo-ethylene glycol
Thanks for the info.
However, I found that the ditosylate of Diethylene glycol is sold at sigma-a ... |
24-5-2007 at 09:10
by: Dr. Beaker |
synthetic chalange regarding oligo-ethylene glycol
Hi all,
I'm interested in making the compound: H2N-(CH2)2[O(CH2)2]3-NH2 (i.e - 4 condensed units ... |
24-5-2007 at 07:33
by: Dr. Beaker |
Triiodobenzoic acid
In three words:
Metal-halogen exchange.
btw - burning in alkaline environment wont help, since H ... |
21-5-2007 at 14:35
by: Dr. Beaker |
Chlorate as a Ligand
in clorate you can say each oxygen bares 1/3 of the negative charge. the lone pair of clorine, and t ... |
15-5-2007 at 10:52
by: Dr. Beaker |
Making phosphorous acid?
E0 of a reaction only tells you something about its thermodynamics, but nothing on the kinetics, or ... |
1-5-2007 at 14:33
by: Dr. Beaker |
synthesis of dimethyl zinc
After considering it - I can use diethyl zinc, however it may affect some aspects of my next steps. ... |
28-4-2007 at 14:33
by: Dr. Beaker |
synthesis of dimethyl zinc
btw - 50 ml 2M sulution in toluene costs about 350$ at aldrich...
so this is a synthesis worth doin ... |
27-4-2007 at 00:51
by: Dr. Beaker |
synthesis of dimethyl zinc
Nicodem - thanx for your usefull input. I need it without ether, since it can interfeer with one of ... |
27-4-2007 at 00:47
by: Dr. Beaker |
synthesis of dimethyl zinc
how can I seperate the ether from the ZnMe2? considering their close b.p
I was thinking to make the ... |
26-4-2007 at 23:34
by: Dr. Beaker |
solubility in organic solvent
as said above, for a specific case consult the lit!!
If you don't find your need there you can use ... |
26-4-2007 at 14:42
by: Dr. Beaker |
synthesis of dimethyl zinc
Hi all,
I need to make ZnMe2, and have ZnCl2 and MeLi*LiBr in ether at my disposal. I think salt ... |
22-4-2007 at 14:42
by: Dr. Beaker |
Cobalt oxide??
If O2 is such a problem then why not do it under inert conditions!? |
22-4-2007 at 12:50
by: Dr. Beaker |
Interesting reactions (KCl melt) / Salt Fusions
At high temp. ("entropy driven rxns") carbon is an efficient reducing agent. So- you may have reduct ... |
7-4-2007 at 12:07
by: Dr. Beaker |
Making uranium metal and thorium metal
maybe a (controled) thermolysis of the azide?
I know NaN3 decompose to Na metal and dinitrogen, so ... |
23-3-2007 at 05:37
by: Dr. Beaker |
Making uranium metal and thorium metal
[quote][i]Originally posted by woelen[/i]
Is uranium really as reactive as calcium? I understood th ... |
22-3-2007 at 09:46
by: Dr. Beaker |
I want some cyanide to play with!
Talukdar, S.; Hsu, J.-L.; Chou, T.-C.; Fang, J.-M.. Direct transformation of aldehydes to nitriles ... |
4-3-2007 at 01:11
by: Dr. Beaker |
| [Next Page] |
