Comments on: Oxime formation from hydroxylamine and ketone: a (computational) reality check on stage one of the mechanism. http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779 Chemistry with a twist Thu, 13 Jun 2013 15:16:09 +0000 hourly 1 http://wordpress.org/?v=3.5.1 By: Intermediates in oxime formation from hydroxylamine and propanone: now you see them, now you don’t. « Henry Rzepa http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779&cpage=1#comment-51625 Intermediates in oxime formation from hydroxylamine and propanone: now you see them, now you don’t. « Henry Rzepa Sun, 14 Apr 2013 18:26:14 +0000 http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779#comment-51625 [...] I revisit the formation of an oxime from hydroxylamine and propanone, but with one change. In the earlier post, I used two molecules of water to achieve the desired proton transfer. Now I look to see what [...]

]]> By: Thalidomide. The role of water in the mechanism of its aqueous racemisation. « Henry Rzepa http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779&cpage=1#comment-12494 Thalidomide. The role of water in the mechanism of its aqueous racemisation. « Henry Rzepa Sat, 10 Nov 2012 22:00:21 +0000 http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779#comment-12494 [...] Oxime formation from hydroxylamine and ketone: a (computational) reality check on stage one of the m… [...]

]]> By: Oxime formation from hydroxylamine and ketone. Part 2: Elimination. « Henry Rzepa http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779&cpage=1#comment-11224 Oxime formation from hydroxylamine and ketone. Part 2: Elimination. « Henry Rzepa Tue, 25 Sep 2012 14:34:20 +0000 http://www.ch.imperial.ac.uk/rzepa/blog/?p=7779#comment-11224 [...] Henry Rzepa Chemistry with a twist « Oxime formation from hydroxylamine and ketone: a (computational) reality check on stage one of the m… [...]

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