09-12-02 12:25
No 355674
Tetrahedron Letters, Volume 35, Issue 48, 28 November 1994, Pages 9099-9100
http://www.sciencedirect.com/cache/Miami
Okay - what can we do with a phenylacetohydroximoyl chloride, which is the product in this rxn?
(Stoni's sexual toy)
09-12-02 12:53
No 355677
Convert it into a nitrile?
I'm not fat just horizontally disproportionate.
(Distinctive Doe)
09-12-02 14:49
No 355708
seems to me there's got to bee an easy way to amphetamine from that.
Check these out.
Tetrahedron (1999), 55(34), 10497-10510.
Tetrahedron Letters (1998), 39(20), 3233-3236.
Tetrahedron Letters (1996), 37(35), 6407-6408.
Patent EP414391
Patent WO9523793
Read and Listen!!! http://www.zmag.org/chomsky/index.cfm
(BusyBee)
09-19-02 13:22
No 358200
I believe that the product of the oximinyl chloride and acetylene, the oxazole would be interesting
something sorta kinda like what you get by cyclizing eph with cyanogen bromide but wrapped around the other way
(forgive me, please as I am on vacation and away from my resources)
but generally cyclic str's (ifn they fit are better yes?) bind better lower entropy and all that
but that is just rampant speculation
(Hive Bee)
09-19-02 13:25
No 358203
nitrostyrenes ---> phenylnitroethanes Bookmark Edit Reply
J. Chem Soc, Perkin Transactions 1,1998, p. 501-4
Mechanism of the yeast mediated reduction of nitrostyrenes in light petroleum
McAnda, Roberts, Smallridge, Ten and Trewhella.
Too good to be true?
(Chief Bee)
09-19-02 17:41
No 358307
Psycosmo: See for yourself, that article is available at http://www.rsc.org/CFmuscat/intermediate
If you UTFSE for "yeast reduction", you will find this topic discussed before among the 55 hits.
(Hive Bee)
09-19-02 18:43
No 358333
Guess I let my exctiment get the better of me