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Amino alcohol via Akabori, trial run [b]From here on no more schizophrenic third person writing or use of acronyms of the SWIM-type will ... |
19-2-2008 at 11:16 by: Nicodem |
Alkaloid Extraction Confirmation? [quote][i]Originally posted by Sauron[/i]
Well, he didn't really come out and say just what his alk ... |
19-2-2008 at 02:41 by: Nicodem |
synthesis of Allantoic acid A quick literature search revealed that allantoic acid is prepared by partial hydrolysis of allantoi ... |
19-2-2008 at 01:09 by: Nicodem |
Amines from alcohols?? Shemati, do you have any references for any kind of Mitsunobo nucleophilic substitution on such a st ... |
19-2-2008 at 01:01 by: Nicodem |
Amines from alcohols?? [quote][i]Originally posted by dan_teod[/i]
I am interested to obtain amines from a tertiary (diphe ... |
18-2-2008 at 01:43 by: Nicodem |
synthesis of Allantoic acid What is "diacetic acid"?
Why don't you first search the literature and patents and then ask others ... |
17-2-2008 at 00:57 by: Nicodem |
chlorination Many members consider the rule of "search before post" a must. There already is a dedicated thread:
... |
15-2-2008 at 10:26 by: Nicodem |
ClO2 as a health product [quote][i]Originally posted by not_important[/i]
The apple juice added may reduct the toxicity by r ... |
14-2-2008 at 10:53 by: Nicodem |
acetylsalicylic acid The treatment with charcoal is part of the recrystallization process. Check a book on how recrystall ... |
14-2-2008 at 10:36 by: Nicodem |
Hunig's base The point was that when two liquids are miscible in all ratios (like Et3N/THF, Et3N/CH2Cl2 , iPr2EtN ... |
14-2-2008 at 10:17 by: Nicodem |
Hunig's base Both those amines are liquids in that temperature range and also fairly nonpolar, so your question m ... |
14-2-2008 at 07:50 by: Nicodem |
Drying ethers over P2O5 [quote][i]Originally posted by Klute[/i]
If using THF, could 1,4-butandiol possibly form? I guess t ... |
14-2-2008 at 07:42 by: Nicodem |
acetylsalicylic acid Don't waste your time. Every aniline is brown or otherwise colored unless freshly prepared. The amou ... |
14-2-2008 at 07:23 by: Nicodem |
ClO2 as a health product [quote][i]Originally posted by Adi[/i]
What happens if you mix NaClO2 with H2O and H3O+ (acid)?[/qu ... |
13-2-2008 at 13:01 by: Nicodem |
Synthesis of malonic acid Unfortunately it is not that easy. Me-CO-CCl<sub>2</sub>-CO-Me in the presence of hydrox ... |
13-2-2008 at 12:53 by: Nicodem |
phenylacetonitrile lockdown I find it hypocritical that this now made famous phenylacetonitrile thread was closed while there ar ... |
12-2-2008 at 14:42 by: Nicodem |
Reaction of CC (TCT) w/Carboxylic Acids in Presence of tert Amine Stop this acronym madness already! ![:mad:](./images/smilies/mad.gif)
Why do some people find it so hard to write "cyanuric ch ... |
12-2-2008 at 14:31 by: Nicodem |
6-hydroxy-2-nitrobenzaldehyde I don't have the access to such obscure literature. You can try in Wanted references, though the abs ... |
11-2-2008 at 10:32 by: Nicodem |
Green Methylating agent....comments I've never seen dimethyl carbonate being used for methylating aliphatic amines. It can however be us ... |
11-2-2008 at 10:27 by: Nicodem |
acetylsalicylic acid The workup I advised some ten posts above will do just fine even if you do the reaction solventless ... |
11-2-2008 at 10:20 by: Nicodem |
Synthesis of malonic acid Two posts above I explained why the haloform reaction on acetylacetone yields acetate and chloroform ... |
5-2-2008 at 14:38 by: Nicodem |
methylenation of catechols using NaF I'm not sure, but I think the Me<sub>4</sub>N<sup>+</sup> cation behaves sim ... |
5-2-2008 at 10:38 by: Nicodem |
methylenation of catechols using NaF It is a quite simple case of solvation issue actually. You have an alkali fluoride used as a base. I ... |
5-2-2008 at 00:01 by: Nicodem |
Ephedrine from Propiophenone... You could have tried using the search engine:
https://sciencemadness.org/talk/viewthread.php?tid=39 ... |
4-2-2008 at 23:41 by: Nicodem |
Ether halogenation? Ethers can get alpha-brominated with bromine. In case of diethyl ether, the product would thus be CH ... |
4-2-2008 at 23:37 by: Nicodem |
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