| Search |
| [Next Page] |
3,4,5-trimethoxy-beta-nitrostyrene synthesis
Where's the data you speak of, then? I'm very interested. |
8-1-2005 at 10:24
by: trilobite |
3,4,5-trimethoxy-beta-nitrostyrene synthesis
Rosco, I'm not saying hallucinogens can give no persistent effects. My point is that it has not ... |
8-1-2005 at 00:05
by: trilobite |
Yeah right
Persistent? I don't think so. Besides, that is hardly a question of metabolism anyway. To my kn ... |
7-1-2005 at 02:02
by: trilobite |
BIODIESEL - cheapen your gasoline
The transesterification proceeds stepwise
triglyceride + methanol --> diglyceride + fatty acid ... |
5-1-2005 at 09:44
by: trilobite |
Adipic acid
Maybe one could invest in a suitable grade of nylon and hydrolyse it... and recover the diamine too. |
5-1-2005 at 01:22
by: trilobite |
Bye bye wishful thinking
The abstract is in error, it should read PhCOCCH not PhCOEt. The reaction is a standard alkyne hydra ... |
4-1-2005 at 08:34
by: trilobite |
Propiophenone rearrangement
Stupid me. Of course I calculated the reaction enthalpy the wrong way around. You're right Kine ... |
3-1-2005 at 11:12
by: trilobite |
Propiophenone rearrangement
Kinetic: It is an oxidation, this was recognized already, but when you look at the proportions of th ... |
2-1-2005 at 08:41
by: trilobite |
Propiophenone rearrangement
I haven't been to my trusty old library for a while, so I haven't checked out the old Beri ... |
2-1-2005 at 08:24
by: trilobite |
Ethyl ether distillation and synthesis
Yes, aldol condensation. In the case of acetone condensing with itself the reaction is: CH3-CO-CH3 + ... |
1-1-2005 at 20:59
by: trilobite |
Propiophenone rearrangement
It looks like the mechanism can be explained with the one in that article very well, but it tells us ... |
1-1-2005 at 19:35
by: trilobite |
Your royal highness
Effect of various acids at different concentrations on the pinacol rearrangement, Tetrahedron Letter ... |
1-1-2005 at 16:28
by: trilobite |
What happened to rhodium and Hive
Some time ago the web site of the Chechen rebels, http://www.kavkazcenter.com , got closed pretty mu ... |
1-1-2005 at 14:06
by: trilobite |
Ethyl ether distillation and synthesis
It could also be the denaturants, which are often ketones such as acetone, MEK or methyl isobutyl ke ... |
30-12-2004 at 19:10
by: trilobite |
3,4,5-trimethoxy-beta-nitrostyrene synthesis
I'm not looking for an argument. This is a matter of theory vs. practice, theoretically it can ... |
29-12-2004 at 16:33
by: trilobite |
3,4,5-trimethoxy-beta-nitrostyrene synthesis
Then there's the cold way of doing the Knoevenagel condensation where the benzaldehyde is disso ... |
29-12-2004 at 15:16
by: trilobite |
3,4,5-trimethoxy-beta-nitrostyrene synthesis
But that's why you should be refluxing it under a condenser and not evaporating in an open flas ... |
29-12-2004 at 14:53
by: trilobite |
3,4,5-trimethoxy-beta-nitrostyrene synthesis
Never forget PIHKAL.
http://www.erowid.org/library/books_online/pihkal/pihkal096.shtml |
29-12-2004 at 14:39
by: trilobite |
Propiophenone rearrangement
Bz stands for benzoyl aka PhCO, which makes BzCOMe phenyl-1,2-propanedione. PhCOEt is propiophenone, ... |
13-12-2004 at 10:35
by: trilobite |
What happened to rhodium and Hive
Yes, I made a mistake, so there's no disagreement! |
10-12-2004 at 00:31
by: trilobite |
What happened to rhodium and Hive
I disagree. The Hive has a different culture, but it certainly has it's sides. Think of the lit ... |
9-12-2004 at 06:38
by: trilobite |
styrene -> something interesting
Wow... that's interesting. I think the hydrolysis part is quite hard to fuck up if one has any ... |
21-11-2004 at 16:04
by: trilobite |
Ethyl Iodide
Maybe the latter of these two methods could be adapted for ethyl iodide as well. Why waste phosphoru ... |
12-11-2004 at 15:01
by: trilobite |
An improved Filter-pump
A few weeks ago I got inspired by this thread, even as there were no practical designs posted, and l ... |
10-9-2004 at 00:09
by: trilobite |
Warning about OTC solvants
I wouldn't be afraid of acetone leaving behind an explosive peroxide residue unless the acetone ... |
14-8-2004 at 08:32
by: trilobite |
| [Next Page] |
