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Mar 26, 2017 at 11:56 history edited orthocresol CC BY-SA 3.0
edited body; edited title
Apr 2, 2015 at 18:41 history edited M.A.R. CC BY-SA 3.0
Fixed image size.
Sep 2, 2014 at 5:58 vote accept Dissenter
Aug 30, 2014 at 0:21 answer added ron timeline score: 11
Aug 28, 2014 at 15:15 comment added Dissenter That's quite an endorsement for Greg's pathway!
Aug 28, 2014 at 15:13 comment added jerepierre I like your second route better, but you still have to worry about E2 competing with SN2 in the last step. Greg E.'s suggestion below is likely the best, which is WW's favorite route.
Aug 28, 2014 at 14:47 history edited Dissenter CC BY-SA 3.0
added 116 characters in body
Aug 28, 2014 at 12:44 comment added Klaus-Dieter Warzecha Supposed that the tosylation of ephedrine works as expected, there still the chance to end up with 1,3-dimethyl-2-phenylaziridine upon heating of the tosylate.
Aug 28, 2014 at 10:20 comment added Klaus-Dieter Warzecha Did you take the tosylation of the secondary amine as a possible side reaction into account? ;)
Aug 28, 2014 at 8:12 history tweeted twitter.com/#!/StackChemistry/status/504904434745606144
Aug 28, 2014 at 6:54 history edited Greg E.
edited tags
Aug 28, 2014 at 6:09 history edited Dissenter CC BY-SA 3.0
added 60 characters in body
Aug 28, 2014 at 6:06 answer added Greg E. timeline score: 16
Aug 28, 2014 at 4:59 history edited Dissenter CC BY-SA 3.0
edited tags; edited title
Aug 28, 2014 at 4:52 history edited Dissenter CC BY-SA 3.0
added 81 characters in body
Aug 28, 2014 at 4:46 history asked Dissenter CC BY-SA 3.0