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Topic: retrosynthesis reactions  (Read 4954 times)

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bob17275

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retrosynthesis reactions
« on: March 12, 2006, 07:03:24 PM »
Could someone help me out with this problem to propose logical synthetic routes to get to the following compounds see attachment diagram..
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Offline barcrphd

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Re:retrosynthesis reactions
« Reply #1 on: March 12, 2006, 11:28:29 PM »
where is the diagram? i cannot see it.
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bob17275

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Re:retrosynthesis reactions
« Reply #2 on: March 13, 2006, 07:29:59 AM »
sorry, the attachment was in jpg but here it is in gif
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Offline Albert

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Re:retrosynthesis reactions
« Reply #3 on: March 13, 2006, 09:29:23 AM »
Check out this hint for question a.
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Pelle

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Re:retrosynthesis reactions
« Reply #4 on: March 14, 2006, 07:00:07 AM »
Albert: I don't really get the reaction with CH3I and OH-. Does that reaction have a name so I can look it up?
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Offline Albert

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Re:retrosynthesis reactions
« Reply #5 on: March 14, 2006, 07:48:01 AM »
No, I don't think it has. To be honest, I think I wrote it not as it ought to: first of all you remove a proton from the derivative of cyclohexanone with a base (that's easy because it yield three limit structures, at least). Then you make it reacting with CH3I: that's an SN2 reaction.
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