Talk:Weinreb ketone synthesis

Latest comment: 9 years ago by Zalumon in topic Better use MeNH(OMe) instead of MeO(Me)NH?
Good articleWeinreb ketone synthesis has been listed as one of the Natural sciences good articles under the good article criteria. If you can improve it further, please do so. If it no longer meets these criteria, you can reassess it.
Article milestones
DateProcessResult
January 17, 2011Good article nomineeListed

somebody created N,O-dimethylhydroxylamine --Stone (talk) 19:38, 19 March 2008 (UTC)Reply

I put in a significant amount of effort to update this page as a part of a class project. I'll be slowly fixing it up over time to better match the MoS. Mdlevin (talk) 05:37, 28 November 2010 (UTC)Reply

GA Review

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This review is transcluded from Talk:Weinreb ketone synthesis/GA1. The edit link for this section can be used to add comments to the review.

Reviewer: Tea with toast (talk) 03:08, 15 January 2011 (UTC)Reply

Issues needing to be addressed

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There are a few issues that need to be addressed before I can pass this article:

  1. Titles should be provided for the journal articles listed in the references.
  2. There might be a problem with consistency in the notation for one of the compounds mentioned in the "Prepartation" section. [MeO(Me)NH•HCl] is mentioned in the text, but the notation of the compound given in the diagram gives [MeONHMe·HCl]. I am assuming that this is the same compound, but the notation should be the same for consistency. Also, further in the article, the compound [MeNH(OMe)·HCl] is given. Does this refer to the same compound as well?

I will place this article on hold for about a week or so for these issues needing to be addressed. Happy editing! --Tea with toast (talk) 19:59, 16 January 2011 (UTC)Reply

Hello! Thanks for your time reviewing the article! I'll go ahead and fix those issues.
  • The journal names are a quick fix and I'll take care of that ASAP.
  • As for the three different ways of writing methoxymethylamine, all refer to the same compound and fixing it shouldn't be an issue either. However, is there one of the ways of writing the reagent that you think would be the best?
M.Levin 20:13, 16 January 2011 (UTC)Reply
So I went ahead and made the changes and chose MeO(Me)NH as the one way to refer to the reagent. I also made a few other minor changes and additions that I had been eyeing. I hope everything is up to par. Please let me know if there's anything else you'd like me to take care of! M.Levin 23:52, 16 January 2011 (UTC)Reply

Final review

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GA review – see WP:WIAGA for criteria

  1. Is it reasonably well written?
    A. Prose quality:  
    B. MoS compliance for lead, layout, words to watch, fiction, and lists:  
  2. Is it factually accurate and verifiable?
    A. References to sources:  
    B. Citation of reliable sources where necessary:  
    C. No original research:  
  3. Is it broad in its coverage?
    A. Major aspects:  
    B. Focused:  
  4. Is it neutral?
    Fair representation without bias:  
  5. Is it stable?
    No edit wars, etc:  
  6. Does it contain images to illustrate the topic?
    A. Images are copyright tagged, and non-free images have fair use rationales:  
    B. Images are provided where possible and appropriate, with suitable captions:  
  7. Overall:
    Pass or Fail:  

Great job! --Tea with toast (talk) 03:32, 17 January 2011 (UTC)Reply

Better use MeNH(OMe) instead of MeO(Me)NH?

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The current notation looks to me as if both methyl groups were attached to the oxygen. Zalumon (talk) 09:18, 10 October 2015 (UTC)Reply