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de-sulfanomidination?
Oh ok so hydrides are out of the question but still you would need hydrogen gas since the carbon fro ... |
17-8-2009 at 19:01
by: sergide |
The taste of salts
Oh yeah that's another thing... it burns but it feels kind of cold, obviously it's used in snowpacks ... |
17-8-2009 at 12:59
by: sergide |
What is the simplest way to reduce a carboxyl group?
Alright, thanks a lot.
Also, what about if like I were to change that -OH to a -Cl using phospho ... |
17-8-2009 at 12:58
by: sergide |
What is the simplest way to reduce a carboxyl group?
What is the simplest way to reduce a carboxyl group (R-COOH) to a methyl group (R-CH3)? |
17-8-2009 at 02:17
by: sergide |
de-sulfanomidination?
Interesting, ok thanks. So hydrogenating it with hydrogen gas with raney nickel...
So then I can ... |
16-8-2009 at 20:56
by: sergide |
2,5-dimethoxybenzaldehyde solubility data
It probably doesn't help but [url=http://www.erowid.org/library/books_online/pihkal/pihkal020.shtml] ... |
16-8-2009 at 18:39
by: sergide |
The taste of salts
Nobody here has tried pure ammonium nitrate? It's interesting, it's a very sour salty which kind of ... |
16-8-2009 at 16:06
by: sergide |
de-sulfanomidination?
Perhaps I should have posted this in "beginnings" since this must be extremely easy for everyone els ... |
16-8-2009 at 15:51
by: sergide |
de-sulfanomidination?
I was wondering: say you have a compound with a sulfanomide side chain. Is it possible to cleave the ... |
16-8-2009 at 12:23
by: sergide |
