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Talk:Amine alkylation

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issues

[edit]

There are some issues with the most recent edits

  • images removed (again) they were already moved from the amine article. deal with the fact that wikipedia contains images, they are added value. The replacement text is also confusing: R'2H2NX ?
  • this entry should be about the synthesis of amines by amine alkylation, it should not be about how to make amines NOT using amine alkylation: that is silly, use the amine page for that.
  • How can it possibly be argued that amine alkylation is not relevant to industry. On account of Ullmann? I am looking at Clopidogrel , Fexofenadine and Quetiapine all drugs in the top-10 blockbuster drugs with a combined turnover of billions of dollars and all drugs containing a tertiary amine that I have good reason to believe all constructed using amines and organohalides in one of the synthetic steps. If you write somewhere something is important or non-important really make sure you have the sources (based on more than just Ullmann).

V8rik (talk) 19:44, 29 March 2010 (UTC)[reply]